KR101102702B1 - The method of reinforcing saponin in ginseng extract - Google Patents
The method of reinforcing saponin in ginseng extract Download PDFInfo
- Publication number
- KR101102702B1 KR101102702B1 KR1020110028294A KR20110028294A KR101102702B1 KR 101102702 B1 KR101102702 B1 KR 101102702B1 KR 1020110028294 A KR1020110028294 A KR 1020110028294A KR 20110028294 A KR20110028294 A KR 20110028294A KR 101102702 B1 KR101102702 B1 KR 101102702B1
- Authority
- KR
- South Korea
- Prior art keywords
- ginseng
- red ginseng
- extract
- saponin
- food
- Prior art date
Links
- 229930182490 saponin Natural products 0.000 title claims abstract description 44
- 150000007949 saponins Chemical class 0.000 title claims abstract description 44
- 239000001397 quillaja saponaria molina bark Substances 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 23
- 235000020710 ginseng extract Nutrition 0.000 title description 3
- 230000003014 reinforcing effect Effects 0.000 title 1
- 235000002789 Panax ginseng Nutrition 0.000 claims abstract description 57
- 235000008434 ginseng Nutrition 0.000 claims abstract description 43
- 241000208340 Araliaceae Species 0.000 claims abstract description 42
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 claims abstract description 42
- 235000003140 Panax quinquefolius Nutrition 0.000 claims abstract description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 239000006228 supernatant Substances 0.000 claims abstract description 10
- 108091005804 Peptidases Proteins 0.000 claims abstract description 6
- 239000004365 Protease Substances 0.000 claims abstract description 6
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims abstract description 6
- 239000006227 byproduct Substances 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 102000004139 alpha-Amylases Human genes 0.000 claims abstract description 3
- 108090000637 alpha-Amylases Proteins 0.000 claims abstract description 3
- 229940024171 alpha-amylase Drugs 0.000 claims abstract description 3
- 239000002994 raw material Substances 0.000 claims description 22
- 238000000605 extraction Methods 0.000 claims description 7
- 239000002244 precipitate Substances 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 abstract description 58
- 108090000790 Enzymes Proteins 0.000 abstract description 58
- 229940088598 enzyme Drugs 0.000 abstract description 58
- 235000013305 food Nutrition 0.000 abstract description 42
- 239000000463 material Substances 0.000 abstract description 3
- 238000010521 absorption reaction Methods 0.000 abstract description 2
- 238000001816 cooling Methods 0.000 abstract 1
- 235000017709 saponins Nutrition 0.000 description 39
- 235000019441 ethanol Nutrition 0.000 description 10
- 238000004128 high performance liquid chromatography Methods 0.000 description 10
- 238000010586 diagram Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- AGBCLJAHARWNLA-DQUQINEDSA-N Ginsenoside RG2 Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]1[C@H](O[C@@H]2[C@H]3C(C)(C)[C@@H](O)CC[C@]3(C)[C@@H]3[C@@]([C@@]4(CC[C@@H]([C@H]4[C@H](O)C3)[C@@](C)(O)CCC=C(C)C)C)(C)C2)O[C@H](CO)[C@@H](O)[C@@H]1O AGBCLJAHARWNLA-DQUQINEDSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000012046 mixed solvent Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 102000013142 Amylases Human genes 0.000 description 4
- 108010065511 Amylases Proteins 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 239000004382 Amylase Substances 0.000 description 3
- 108010059892 Cellulase Proteins 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 102000004882 Lipase Human genes 0.000 description 3
- 108090001060 Lipase Proteins 0.000 description 3
- 239000004367 Lipase Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YURJSTAIMNSZAE-UHFFFAOYSA-N UNPD89172 Natural products C1CC(C2(CC(C3C(C)(C)C(O)CCC3(C)C2CC2O)OC3C(C(O)C(O)C(CO)O3)O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O YURJSTAIMNSZAE-UHFFFAOYSA-N 0.000 description 3
- 238000007259 addition reaction Methods 0.000 description 3
- 235000019418 amylase Nutrition 0.000 description 3
- 229940106157 cellulase Drugs 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 229930182494 ginsenoside Natural products 0.000 description 3
- 235000019421 lipase Nutrition 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- AGBCLJAHARWNLA-UHFFFAOYSA-N (20R)-ginsenoside Rg2 Natural products OC1C(O)C(O)C(C)OC1OC1C(OC2C3C(C)(C)C(O)CCC3(C)C3C(C4(CCC(C4C(O)C3)C(C)(O)CCC=C(C)C)C)(C)C2)OC(CO)C(O)C1O AGBCLJAHARWNLA-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000011033 desalting Methods 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 235000013376 functional food Nutrition 0.000 description 2
- 229940089161 ginsenoside Drugs 0.000 description 2
- YURJSTAIMNSZAE-HHNZYBFYSA-N ginsenoside Rg1 Chemical compound O([C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(C[C@@H]([C@H]4C(C)(C)[C@@H](O)CC[C@]4(C)[C@H]3C[C@H]2O)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C)(C)CC1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O YURJSTAIMNSZAE-HHNZYBFYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- JURZHOVRCOWZFN-UHFFFAOYSA-N notoginsenoside R1 Natural products CC(=CCCC(C)(OC1OC(CO)C(O)C(O)C1O)C2CCC3(C)C2C(O)CC4C5(C)CCC(O)C(C)(C)C5C(CC34C)OC6OC(COC7OCC(O)C(O)C7O)C(O)C(O)C6O)C JURZHOVRCOWZFN-UHFFFAOYSA-N 0.000 description 2
- 238000009938 salting Methods 0.000 description 2
- RWXIFXNRCLMQCD-JBVRGBGGSA-N (20S)-ginsenoside Rg3 Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@H]1CC[C@]2(C)[C@H]3C[C@@H](O)[C@H]4[C@@]([C@@]3(CC[C@H]2C1(C)C)C)(C)CC[C@@H]4[C@@](C)(O)CCC=C(C)C)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O RWXIFXNRCLMQCD-JBVRGBGGSA-N 0.000 description 1
- 235000019750 Crude protein Nutrition 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 240000004371 Panax ginseng Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000010170 biological method Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- OORMXZNMRWBSTK-LGFJJATJSA-N dammarane Chemical group C1CCC(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@H]([C@H](C)CCCC(C)C)[C@H]4CC[C@@H]3[C@]21C OORMXZNMRWBSTK-LGFJJATJSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003648 triterpenes Chemical class 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
Images
Classifications
-
- 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
- A23L2/02—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation containing fruit or vegetable juices
- A23L2/04—Extraction of juices
-
- 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
-
- 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
-
- 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
- A23V2250/2124—Ginseng
Landscapes
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicines Containing Plant Substances (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
본 발명은 인삼 및 홍삼 액기스의 사포닌 함량을 높이는 방법에 관한 것으로 더욱 상세하게는 진세노사이드 Rg1, Rg2, Rg3 등의 Rg계열 사포닌 함량을 높이는 방법에 관한 것이다. The present invention relates to a method for increasing the saponin content of ginseng and red ginseng extract, and more particularly, to a method for increasing the content of Rg-based saponins such as ginsenosides Rg1, Rg2, and Rg3.
인삼 및 홍삼의 유효성분은 진세노사이드로 명명되는 사포닌으로, 트리터르페노이드(triterpenoid)의 담마란(dammarane) 골격을 가진 글리코시드의 구조를 갖는다. 특히 고려인삼(Panax ginseng)에는 30여종의 사포닌 성분이 알려져 있고, 이러한 사포닌 성분들은 각각 다양한 약효를 나타내고, 그 구조에 따라 약효의 종류와 강도가 다르게 나타난다.The active ingredients of ginseng and red ginseng are saponins called ginsenosides, and have a structure of glycosides having a dammarane skeleton of triterpenoids. In particular, ginseng (Panax ginseng) 30 kinds of saponin components are known, these saponin components each exhibit a variety of drugs, depending on the structure and the type and strength of the drug appears different.
최근 인삼 및 홍삼에 함유된 사포닌이 의약품, 화장품 및 기능성 식품소재 등으로의 수요가 증가되고 있으며, 특히 화장품과 식품소재로 사용할 때 유해성이 소비자들의 구매요건에 민감한 요소로 작용할 수 있어, 인체에 무해한 소재를 사용하는 친환경적인 인삼 및 홍삼에 함유된 사포닌의 함량을 높이는 방법이 요구되고 있다. 또한 무해함에 더해 보다 우수한 생리활성을 지닌 액기스 제품의 요구도 꾸준히 증가하고 있는 추세이다. Recently, saponins contained in ginseng and red ginseng are increasing in demand for medicines, cosmetics, and functional foods.In particular, when used as cosmetics and foods, harmfulness may act as a sensitive factor to consumers' purchase requirements, which is harmless to humans. There is a need for a method of increasing the content of saponins contained in environmentally friendly ginseng and red ginseng using materials. In addition to the harmlessness, the demand for extract products with better physiological activity is steadily increasing.
상기와 같이 인삼 및 홍삼에 함유된 사포닌을 증강시키는 기술에 관한 문헌으로는 우선 등록특허 10-0620107를 들 수 있는데, 이는 홍삼, 수삼, 백삼 또는 이의 부산물로 이루어진 군 중에서 선택된 적어도 하나 이상을 물, 에탄올 또는 이들의 혼합용매로 추출하는 제1단계와;Documents relating to the technology for enhancing the saponin contained in ginseng and red ginseng as described above may be first registered Patent 10-0620107, which is water, at least one selected from the group consisting of red ginseng, ginseng, white ginseng or by-products thereof Extracting with ethanol or a mixed solvent thereof;
상기 추출물을 85~105 ℃로 3 내지 10시간 동안 가열처리하거나 또는 상기 추출물에 추출물 중량의 약 1 ~ 10배 부피의 초산, 구연산 또는 젖산 용액으로 구성된 그룹에서 선택된 10~50(v/w)% 약산을 가하여 pH 2.5 내지 4.0이 되도록 하고 70 ~ 90℃에서 1 내지 10시간 동안 가열 환류 처리함으로써 약산처리하는 제2단계와;10 to 50 (v / w)% selected from the group consisting of the extract is heat-treated at 85 ~ 105 ℃ for 3 to 10 hours or a solution of acetic acid, citric acid or lactic acid in a volume of about 1 to 10 times the weight of the extract in the extract Adding a weak acid to a pH of 2.5 to 4.0 and performing a weak acid treatment by heating to reflux at 70 to 90 ° C. for 1 to 10 hours;
상기 처리된 추출물을 물과 에탄올의 혼합용매에 용해시켜 침전물은 제거하고 상층액을 수집하는 제3단계와; Dissolving the treated extract in a mixed solvent of water and ethanol to remove the precipitate and collecting the supernatant;
상기 상층액을 물, 에탄올 또는 이들의 혼합용매를 전개용매로 사용하여 다공성수지 컬럼크로마토그래피로 정제하는 제4단계와;A fourth step of purifying the supernatant by porous resin column chromatography using water, ethanol or a mixed solvent thereof as a developing solvent;
상기 진세노사이드 Rg2의 함량이 50% 이상인 분획물을 수집, 농축하고, 4단계의 정제하는 과정을 수회 반복하여 진세노사이드 Rg2를 제조하는 제5단계로 구성되는 것을 특징으로 한다.
The fifth step of preparing ginsenoside Rg2 by collecting and concentrating a fraction having a content of ginsenoside Rg2 of 50% or more and repeating four steps of purification.
또 다른 문헌인 등록특허 10-0780056은 원료를 물에서 열수추출하고 농축하여 얻어진 농축액에 알코올류를 가하여 침전된 이물질을 제거하는 단계와; 염석제를 투여하여 포화농도 하에 얻어진 침전물을 물에 재용해시키는 단계와; 그래디언트 염석법을 시행하여 각기 다른 염석제 농도마다 차등 침전물을 얻은 단계와; 상기 침전물을 분석하여 인삼 사포닌 Rg2 집중부분과 비집중부분으로 구분하는 단계와; 인삼 사포닌 Rg2 집중부분만을 취하여 탈염제로 탈염 및 탈색하고 농축한 후 다시 메틸알코올, 에틸알코올, 이소프로필알코올, 아밀알코올 중에서 선택된 알코올류로 정제하여 재결정화하는 단계로 구성된 인삼사포닌의 제조방법에 관한 것이다.
Another document 10-0780056 is a step of removing foreign matter precipitated by adding alcohol to the concentrate obtained by hot water extraction and concentration of the raw material in water; Administering a salting agent to redissolve the precipitate obtained under saturation in water; Performing a gradient salting method to obtain differential precipitates at different salt concentrations; Analyzing the precipitate and dividing the ginseng saponin Rg2 into concentrated and non-concentrated portions; Ginseng saponin Rg2 concentrated portion of the ginseng saponin comprising the step of desalting and decolorizing with a desalting agent, concentrated and then recrystallized by re-crystallization with alcohols selected from methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol. .
그러나 상기와 같은 인삼 및 홍삼액기스의 제조방법은 주로 인삼 또는 홍삼을 주정 혹은 열수추출하고 이렇게 얻어진 당과 조사포닌의 혼합물을 농축하여 얻는 방법에 관한 것으로 전체 액기스에서 차지하는 사포닌의 함량이 매우 낮다. 이는 인삼의 식품으로서의 특성을 무시하고 사포닌 전환을 단순한 화학적인 방법에만 의존했기 때문이다. 이에 본 발명자들은 기존의 화학적인 추출방법 외에 효소를 사용한 생물학적인 방법을 사용하면 보다 효과적으로 인삼 사포닌의 함량을 높일 수 있을 것이라는 점에 착안하여 본 발명과 관련된 연구를 진행하였다.
However, the manufacturing method of the ginseng and red ginseng extract as described above mainly relates to a method of obtaining by distilling ginseng or red ginseng extract or hot water and concentrating the mixture of the sugar and the irradiated saponins obtained in this way is very low in the total saponin content. This is due to the fact that ginseng disregards its food characteristics and relies on saponin conversion only by simple chemical methods. Therefore, the present inventors proceeded with the research related to the present invention focusing on the fact that using a biological method using an enzyme in addition to the conventional chemical extraction method can more effectively increase the content of ginseng saponin.
효소는 대상이 되는 물질 (화학물질 혹은 부산물)에 작용하여 그 물질을 다른 물질로 전환시키며 자기 자신은 변화하지 않는 단백질 분자를 가리킨다. 효소가 작용하는 물질을 특별히 "기질"이라고 한다. 고유의 특성을 지닌 기질은 효소에 의해 다른 특성을 지닌 물질로 바뀌게 된다. 효소는 각기 반응하는 기질과 입체적인 결합을 위해 고유한 모양을 지닌다.Enzymes act on a target substance (a chemical or by-product) to convert the substance into another substance, which in itself refers to a protein molecule that does not change. Substances on which enzymes work are specifically called "substrates." Substrates with their own properties are converted into substances with different properties by enzymes. Enzymes have a unique shape for their three-dimensional bond with the reacting substrate.
효소의 종류가 너무 많기 때문에, 구조적인 명명법이 필요한데, 이것은 National Enzyme Commission이라는 단체에 의하여 고안되었다. 모든 효소의 정식 명칭 뒤에는 "-ase" (한국어로는 "-아제")를 사용한다. 대부분 효소의 명칭은 그 기능을 나타내는 용어로 구성되어 있다. 예를 들어 리파제(lipase)는 기름(lipid)의 일종인 지방(fat)을 분해하는 효소이며, 셀룰라제(cellulase)는 목질계 물질인 셀룰로스(cellulose)를 분해하는 효소이다. 또한 아밀라제(amylase)는 전분을 분해하는데 사용된다.Due to the large number of enzymes, structural nomenclature is required, which was devised by the National Enzyme Commission. The official name of all enzymes is "-ase" ("-ase" in Korean). Most names of enzymes consist of terms that describe their function. For example, lipase is an enzyme that breaks down fat, which is a kind of lipid, and cellulase is an enzyme that breaks down cellulose, a woody substance. Amylase is also used to break down starch.
효소는 우리 인체내에서 섭취된 음식물의 분해와 소화흡수를 돕는 역할을 한다. 따라서 인삼을 섭취하였을 경우에는 이 효소들이 작용하여 인삼의 성분을 분해하여 소화되기 쉬운 형태로 바꾸는 것이다. Enzymes help the digestion and digestion of foods ingested in our bodies. Therefore, when ingested ginseng these enzymes act to break down the components of the ginseng into a digestible form.
본 발명은 음식물의 인체 흡수를 도울 수 있는 식품효소를 인삼 및 홍삼 추출물에 적용하여 인체에 유익한 진세노사이드인 Rg의 함유량을 증진시킨 인삼 및 홍삼 액기스를 간편하고 높은 수율로 수득하고자 한다.The present invention is intended to obtain a simple and high yield of ginseng and red ginseng extract to enhance the content of Rg, a ginsenoside beneficial to the human body by applying a food enzyme that can help human body absorption of food in ginseng and red ginseng extract.
상기한 과제를 해결하기 위하여 본 발명은In order to solve the above problems,
인삼 및 홍삼 액기스의 Rg계열 사포닌 함량을 높이는 방법에 있어서,In the method of increasing the Rg-based saponin content of ginseng and red ginseng extract,
수삼, 백삼, 홍삼 또는 이의 부산물로부터 원료를 선택하는 단계와;Selecting raw materials from fresh ginseng, white ginseng, red ginseng or by-products thereof;
상기 선택된 원료를 혼합용매로 추출하는 단계와;Extracting the selected raw material with a mixed solvent;
상기 추출 단계가 종료된 원료의 온도를 30℃로 내리고 식품효소를 첨가하여 생물학적 전환을 일으키는 단계와;Lowering the temperature of the raw material from which the extraction step is completed to 30 ° C. and adding a food enzyme to cause biological conversion;
상기 생물학적 전환처리된 인삼원료에 물과 에탄올 첨가하여 용해시키는 단계와;Dissolving and adding water and ethanol to the biologically converted ginseng raw material;
상기 용해된 원료의 침전물을 제거하고 상층액을 수집하는 단계와;Removing the precipitate of the dissolved raw material and collecting the supernatant;
상기 수집된 상층액을 가열, 농축하여 진세노사이드 Rg가 강화된 액기스의 형태로 제조하는 단계;로 구성되는 것을 특징으로 한 인삼 및 홍삼 액기스의 Rg계열 사포닌 함량을 높이는 방법을 과제 해결을 위한 수단으로서 제공한다.Heating and concentrating the collected supernatant to prepare a ginsenoside Rg-enriched extract; means for increasing the Rg-based saponin content of ginseng and red ginseng extract, comprising a means for solving the problem. Provided as.
또한 본 발명은 상기한 과제를 보다 효과적으로 해결하기 위하여In addition, the present invention to solve the above problems more effectively
상기 선택된 원료를 혼합용매로 추출하는 단계는 건조된 원료 중량 대비 5~20 배의 물 또는 주정을 이용하여, 70℃~120℃의 온도로 18~30시간 동안 수행되는 것을 특징으로 하는 인삼 및 홍삼 액기스의 Rg계열 사포닌 함량을 높이는 방법을 제공하고,Extracting the selected raw material with a mixed solvent is ginseng and red ginseng, characterized in that carried out for 18 to 30 hours at a temperature of 70 ℃ ~ 120 ℃ using 5 to 20 times the water or alcohol compared to the weight of the dried raw material To provide a method of increasing the content of the Rg-based saponin of the extract,
상기 생물학적 전환을 일으키는 단계는 리파제, 프로테아제, 셀룰라제, 아밀라제 및 이들의 혼합물로부터 선택되는 식품효소를 사용하여 30분간 수행되는 것을 특징으로 한 인삼 및 홍삼 액기스의 Rg계열 사포닌 함량을 높이는 방법을 제공한다.The step of causing the biological conversion provides a method for increasing the Rg-based saponin content of ginseng and red ginseng extract, characterized in that performed for 30 minutes using a food enzyme selected from lipase, protease, cellulase, amylase and mixtures thereof. .
본 발명에 의하면 식품, 의약적 가치가 높은 Rg계열의 사포닌을 다량 함유하는 인삼액기스를 제조함에 있어 인체에 유익한 식품효소를 사용하여 안전하고, 친환경적이며, 제조방법이 간단, 편리하고 경제적이며, 제조수율이 높은 장점이 기대된다.According to the present invention, in the manufacture of ginseng extract containing a large amount of Rg-based saponin of food and medicinal value, it is safe, eco-friendly, simple and convenient, economical, and easy to manufacture using food enzymes beneficial to the human body. High yields are expected.
또한 본 발명의 제조방법으로 제조한 Rg강화 인삼액기스는 식품, 기능성 식품, 화장품 및 의약품 제조시에 안전하게 사용할 수 있다.In addition, Rg-enriched ginseng extract prepared by the manufacturing method of the present invention can be safely used in the manufacture of food, functional food, cosmetics and pharmaceuticals.
도 1은 본 발명의 사포닌 함량을 높인 인삼 및 홍삼 액기스를 제조하는 공정을 나타내는 도면이다.
도 2 내지 도 7은 식품효소의 첨가 반응 시간의 경과에 따른 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면으로서,
도 2는 식품효소가 첨가되지 않은 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.
도 3은 식품효소를 첨가시킨 후 30분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.
도 4는 식품효소를 첨가시킨 후 60분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.
도 5는 식품효소를 첨가시킨 후 90분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.
도 6은 식품효소를 첨가시킨 후 120분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.
도 7은 식품효소를 첨가시킨 후 150분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면이다.1 is a view showing a process for producing a ginseng and red ginseng extract with a high saponin content of the present invention.
2 to 7 is a diagram showing the saponin content contained in the red ginseng extract with the passage of the reaction time of food enzyme addition by HPLC,
Figure 2 is a diagram showing the saponin content contained in the red ginseng extract not added food enzyme by HPLC.
3 is a diagram showing the saponin content contained in the red ginseng extract reacted for 30 minutes after the addition of food enzymes by HPLC.
4 is a diagram showing the saponin content contained in red ginseng extract reacted for 60 minutes after the addition of food enzymes by HPLC.
5 is a diagram showing the saponin content contained in the red ginseng extract reacted for 90 minutes after the addition of food enzymes by HPLC.
6 is a diagram showing the saponin content contained in red ginseng extract reacted for 120 minutes after the addition of food enzymes by HPLC.
7 is a diagram showing the saponin content contained in the red ginseng extract reacted for 150 minutes after the addition of food enzymes by HPLC.
이하 첨부한 도면과 실시예를 바탕으로 본 발명을 더욱 상세히 설명한다.Hereinafter, the present invention will be described in more detail with reference to the accompanying drawings and examples.
본 발명은 인삼 및 홍삼에 함유된 사포닌을 식품효소를 이용하여 증강시키는 것을 것을 특징으로 한다.The present invention is characterized by enhancing the saponins contained in ginseng and red ginseng using food enzymes.
도 1은 본 발명의 사포닌 함량을 높인 홍삼 액기스를 제조하는 공정을 나타내는 도면이다.1 is a view showing a process for producing a red ginseng extract with a high saponin content of the present invention.
본 발명에 사용되는 원료는 수삼, 백삼, 홍삼 또는 이의 부산물로부터 선택되는 것을 특징으로 한다.The raw material used in the present invention is characterized in that selected from ginseng, white ginseng, red ginseng or by-products thereof.
상기 선택된 원료를 증숙기에 넣고 증숙시킨다. 그런 다음 이를 건조, 숙성하여 원료로 사용한다.The selected raw material is placed in a steamer and steamed. Then, it is dried and aged to use as raw materials.
상기 건조, 숙성된 원료를 절단기로 100~300brix로 세분한다. 상기 세분 또는 세절과정은 하기의 식품효소와의 반응을 원활하게 진행시키기 위함이다. The dried and aged raw material is subdivided into 100 ~ 300brix with a cutter. The subdivision or trituration process is to facilitate the reaction with the following food enzymes.
상기 세절작업이 종료된 원료에 물 또는 주정을 첨가하여 추출한다. 상기 추출은 70℃~120℃의 온도로 18~30시간 추출하는 것이 바람직하지만 반드시 이에 한정되는 것은 아니고 당업자라면 적절히 원료와 투입된 물 또는 주정의 양에 따라 적절히 변경하여 실시할 수 있음은 물론이다. 상기 추출이 완료되면 혼합용액의 온도를 20~40℃로 낮추고 pH를 6.5~7.5으로 조정한다. Extraction is performed by adding water or spirit to the raw material in which the cutting operation is completed. The extraction is preferably carried out for 18 to 30 hours at a temperature of 70 ℃ ~ 120 ℃, but is not necessarily limited to this, those skilled in the art can be appropriately changed according to the amount of raw materials and water or spirits are appropriately performed. When the extraction is completed, lower the temperature of the mixed solution to 20 ~ 40 ℃ and adjust the pH to 6.5 ~ 7.5.
상기 과정을 거친 원료용액에 식품효소를 첨가한다. Food enzyme is added to the raw material solution after the above process.
본 발명에서 사용되는 식품효소는 리파제, 프로테아제, 셀룰라제, 아밀라제 및 이들의 혼합물로부터 선택되는 것을 특징으로 한다. 바람직하게는 본 발명에서 사용되는 식품효소는 전체 중량비 대비 조단백질이 10% 이상이어야 하며, 이중에서 알파 아밀라제와 프로테아제의 활성이 각각 300 단위/mg과 200 단위/mg 이상인 것을 특징으로 한다.The food enzyme used in the present invention is characterized in that it is selected from lipase, protease, cellulase, amylase and mixtures thereof. Preferably, the food enzyme used in the present invention should be at least 10% crude protein relative to the total weight ratio, of which the activity of alpha amylase and protease is characterized in that 300 units / mg and 200 units / mg or more, respectively.
상기 반응이 효소첨가 반응이 종료된 인삼 또는 홍삼액을 다시 가열하여 효소를 실활시키고 이를 농축기에 투입하여 농축시켜 최종적으로 홍삼액기스를 제조한다.
The reaction is heated again to ginseng or red ginseng solution, the enzyme addition reaction is complete to deactivate the enzyme and concentrated by adding it to a concentrator to finally produce a red ginseng extract.
실시예 1: 식품효소를 첨가한 홍삼 액기스의 제조방법Example 1 Preparation of Red Ginseng Extract Added with Food Enzyme
100kg의 수삼을 증숙기에 넣어 90℃ 1.5기압의 압력 하에서 15일간 증숙시켜 홍삼 90kg을 얻었다. 이렇게 얻어진 홍삼을 1개월간 건조하여 수분이 제거된 건조 홍삼 50kg을 수득하였다. 이렇게 얻어진 50kg의 홍삼을 4개월간 숙성하여 최종 홍삼을 제조하여 이를 인삼원료로 사용하였다.100 kg of fresh ginseng was steamed in a steamer for 15 days under a pressure of 1.5 ° C. at 90 ° C. to obtain 90 kg of red ginseng. The red ginseng thus obtained was dried for 1 month to obtain 50 kg of dried red ginseng from which moisture was removed. The 50kg red ginseng thus obtained was aged for 4 months to prepare the final red ginseng, which was used as a ginseng raw material.
상기 방법에 의해 제조된 건조홍삼을 절단기로 100~300brix로 세분한 후 여기에 1ton의 물을 넣고 추출기에서 90℃의 온도로 24시간 추출하였다. 추출이 완료된 후 혼합용액의 30℃로 온도를 낮추고 pH를 7.0으로 조정한 뒤 식품효소 30kg((주)해나눔에서 제조 공급하는 미라클엔자임 아밀라제와 프로테아제의 혼합효소)를 투입하여 30분간 반응시켰다. 상기 반응이 종료된 인삼원료를 물과 에탄올의 혼합물(부피대비 물:에탄올 = 5:1) 500kg을 첨가하여 20시간 동안 용해시킨 후, 침전물을 제거하고 상층액을 수집하였다.The dried red ginseng prepared by the above method was subdivided into 100 ~ 300brix using a cutter, and then 1ton of water was added thereto and extracted at a temperature of 90 ° C. for 24 hours in an extractor. After the extraction was completed, the temperature was lowered to 30 ° C. of the mixed solution, the pH was adjusted to 7.0, and 30 kg of food enzyme (Miracle Enzyme amylase and protease mixed enzyme manufactured by Haenam) was added and reacted for 30 minutes. After completion of the reaction, 500 g of a mixture of water and ethanol (volume of water: ethanol = 5: 1) was added thereto to dissolve for 20 hours, and then the precipitate was removed and the supernatant was collected.
상기 수득된 상층액을 90℃로 가열하여 효소를 실활시키고 이를 농축기에 투입하여 농축시켜 최종적으로 30kg의 홍삼액기스를 제조하였다.
The supernatant obtained above was heated to 90 ° C. to deactivate the enzyme, which was then concentrated in a thickener to finally prepare 30 kg of red ginseng extract.
실시예 2: 식품효소를 첨가한 홍삼액기스의 제조방법Example 2 Preparation of Red Ginseng Extract Added with Food Enzyme
식품효소를 투입하여 60분간 반응시킨 것을 제외하고는 실시예 1과 동일하게 실시하였다.
The same procedure as in Example 1 was carried out except that the food enzyme was reacted for 60 minutes.
실시예 3: 식품효소를 첨가한 홍삼액기스의 제조방법Example 3 Preparation of Red Ginseng Extract Added with Food Enzyme
식품효소를 투입하여 90분간 반응시킨 것을 제외하고는 실시예 1과 동일하게 실시하였다.
The same procedure as in Example 1 was carried out except that the food enzyme was added and reacted for 90 minutes.
실시예 4: 식품효소를 첨가한 홍삼액기스의 제조방법Example 4 Preparation of Red Ginseng Extract Added with Food Enzyme
식품효소를 투입하여 120분간 반응시킨 것을 제외하고는 실시예 1과 동일하게 실시하였다.
The same procedure as in Example 1 was carried out except that the food enzyme was added and reacted for 120 minutes.
실시예 5: 식품효소를 첨가한 홍삼액기스의 제조방법Example 5 Preparation of Red Ginseng Extract Added with Food Enzyme
식품효소를 투입하여 150분간 반응시킨 것을 제외하고는 실시예 1과 동일하게 실시하였다.
The same procedure as in Example 1 was carried out except that the food enzyme was added and reacted for 150 minutes.
비교예 1: 식품효소를 첨가하지 않은 홍삼액기스의 제조방법Comparative Example 1: Preparation of Red Ginseng Extract without Food Enzyme
실시예 1과 동일하게 실시하되 식품효소 대신 추출물 중량의 5배 부피의 초산, 구연산, 젖산 용액 혼합물을 첨가하여 3시간 동안 반응시켰다. 상기 반응이 종료된 홍삼액을 농축기에 투입하여 농축시켜 최종적으로 30kg의 홍삼액기스를 제조하였다.
The reaction was carried out in the same manner as in Example 1, but the reaction was performed for 3 hours by adding a mixture of acetic acid, citric acid and lactic acid solution of 5 times the weight of the extract instead of food enzymes. The red ginseng solution of which the reaction was completed was added to a concentrator and concentrated to finally prepare 30 kg of red ginseng extract.
상기 실시예 1~5와 비교예 1에 의해 제조된 홍삼액기스의 사포닌 함량을 하기 표1과 도2~7을 통해 나타내었다. 전체적으로 식품효소를 첨가한 실시예 1~5의 홍삼액기스에서 모든 사포닌의 함량이 증가됨을 알 수 있다. 특기할 만한 점은 효소반응 30분 경과 후의 사포닌 함량이 가장 높은 것으로 파악되었다. 이는 시간이 경과함에 따라 일부 사포닌의 분해되기 때문인 것으로 풀이된다. 따라서 식품효소의 첨가반응에서 반응시간은 30분정도가 가장 바람직한 것으로 보고되었다.
The saponin content of the red ginseng extract prepared by Examples 1 to 5 and Comparative Example 1 is shown through Table 1 and FIGS. 2 to 7. It can be seen that the content of all saponins in the red ginseng extract of Examples 1 to 5 added with the food enzyme as a whole. It is remarkable that saponin content was the highest after 30 minutes of enzyme reaction. This is believed to be due to the degradation of some saponins over time. Therefore, it was reported that the reaction time of the food enzyme addition reaction was about 30 minutes.
도 2 내지 도 7은 식품효소의 첨가 반응 시간의 경과에 따른 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내는 도면으로서,2 to 7 is a diagram showing the saponin content contained in the red ginseng extract with the passage of the reaction time of food enzyme addition by HPLC,
도 2는 식품효소가 첨가되지 않은 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타내고, 도 3~7은 식품효소를 첨가하여 각각 30분, 60분, 90분, 120분, 150분간 반응시킨 홍삼 액기스에 함유된 사포닌 함량을 HPLC로 나타낸다. 도시된 바와 같이 30분 경과 후 가장 높은 사포닌 피크값을 나타냄을 알 수 있다.
Figure 2 shows the saponin content contained in the red ginseng extract not added food enzyme by HPLC, Figures 3-7 is a red ginseng extract reacted for 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes by adding the food enzyme The saponin content contained in is shown by HPLC. It can be seen that the highest saponin peak value after 30 minutes as shown.
없음none
Claims (3)
수삼, 백삼, 홍삼 또는 이의 부산물로부터 원료를 선택하는 단계와;
상기 선택된 원료의 중량 대비 5~20배의 물 또는 주정을 이용하여 70~120℃의 온도에서 18~30시간 동안 추출하는 단계와;
상기 추출 단계가 종료된 원료의 온도를 30℃로 내리고 활성이 300 단위/mg인 알파 아밀라제와 활성이 200단위/mg인 프로테아제 혼합물을 전체 원료 중량대비 10%이상 투입하여 30분간 반응시켜 생물학적 전환을 일으키는 단계와;
상기 생물학적 전환처리된 원료에 물과 에탄올을 첨가하여 용해시키는 단계와;
상기 용해된 원료의 침전물은 제거하고 상층액을 수집하는 단계와;
상기 수집된 상층액을 가열, 농축하여 진세노이드 Rg가 강화된 액기스의 형태로로 제조하는 단계로 구성되는 것을 특징으로 한 인삼 및 홍삼액기스의 Rg계열 사포닌 함량을 높이는 방법
In the method of increasing the Rg-based saponin content of ginseng and red ginseng extract,
Selecting raw materials from fresh ginseng, white ginseng, red ginseng or by-products thereof;
Extracting at a temperature of 70 to 120 ° C. for 18 to 30 hours using water or alcohol 5 to 20 times the weight of the selected raw material;
The temperature of the raw material after the extraction step is lowered to 30 ° C., and the activity of 300 units / mg of alpha amylase and 200 units / mg of protease mixture is added at least 10% relative to the total weight of the raw material and reacted for 30 minutes for biological conversion. Causing step;
Adding water and ethanol to the biologically converted raw material to dissolve it;
Removing the precipitate of the dissolved raw material and collecting the supernatant;
Method of increasing the Rg-based saponin content of ginseng and red ginseng extract, comprising the step of heating and concentrating the collected supernatant to form a ginsenoid Rg-enhanced extract form
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020110028294A KR101102702B1 (en) | 2011-03-29 | 2011-03-29 | The method of reinforcing saponin in ginseng extract |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020110028294A KR101102702B1 (en) | 2011-03-29 | 2011-03-29 | The method of reinforcing saponin in ginseng extract |
Publications (1)
Publication Number | Publication Date |
---|---|
KR101102702B1 true KR101102702B1 (en) | 2012-01-05 |
Family
ID=45613755
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020110028294A KR101102702B1 (en) | 2011-03-29 | 2011-03-29 | The method of reinforcing saponin in ginseng extract |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101102702B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014007427A1 (en) * | 2012-06-20 | 2014-01-09 | 주식회사 한국야쿠르트 | Method using enzyme conversion and lactobacillus fermentation for preparing concentrated fermented red ginseng liquid having enhanced compound k content, and product containing concentrated fermented red ginseng liquid prepared by said preparation method as active ingredient |
KR101429272B1 (en) | 2012-06-15 | 2014-09-24 | (주)바이오벤 | Methods for Extracting Active Ingredients from Ginseng |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20090050654A (en) * | 2007-11-16 | 2009-05-20 | 주식회사 케이티앤지 | Preparing methods of red ginseng extracts comprising protopanaxatriol saponins as high density |
-
2011
- 2011-03-29 KR KR1020110028294A patent/KR101102702B1/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20090050654A (en) * | 2007-11-16 | 2009-05-20 | 주식회사 케이티앤지 | Preparing methods of red ginseng extracts comprising protopanaxatriol saponins as high density |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101429272B1 (en) | 2012-06-15 | 2014-09-24 | (주)바이오벤 | Methods for Extracting Active Ingredients from Ginseng |
WO2014007427A1 (en) * | 2012-06-20 | 2014-01-09 | 주식회사 한국야쿠르트 | Method using enzyme conversion and lactobacillus fermentation for preparing concentrated fermented red ginseng liquid having enhanced compound k content, and product containing concentrated fermented red ginseng liquid prepared by said preparation method as active ingredient |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107338280B (en) | Low-glycosyl ginseng glucoside group and preparation method of aglycone thereof | |
KR20110104621A (en) | Ginseng fermentation system for ginsenoside increase | |
KR101233987B1 (en) | Manufacturing method of fermentative red ginseng | |
KR101341755B1 (en) | The effective isolation method of panaxadiol saponin fraction from ginseng using pectinase | |
JP4809281B2 (en) | Efficient production method for human salmon extract with high content of red salmon-specific saponin | |
KR20110052940A (en) | A process for preparing an extract fraction enriched with ginsenoside rg3 from ginseng radix | |
KR101176631B1 (en) | A preparation method of processed red ginseng which increases ginsenoside metabolites | |
CN113621673B (en) | Method for fermenting ginseng by composite strain, fermentation product and application | |
KR101106487B1 (en) | A process for preparing an red ginseng extract enriched with ginsenoside rg3 and rh2 | |
KR101102702B1 (en) | The method of reinforcing saponin in ginseng extract | |
KR101877225B1 (en) | Method for Manufacturing Tablet Containing Fermented Ginseng and Maca | |
CN102994309A (en) | Ginkgo-sorghum liquor and ginkgo-sorghum health-care liquor | |
US20200317822A1 (en) | Method for Preparing Arabinogalacturonan from Tangerine Peel | |
CN112370516A (en) | A wall-broken Ganoderma spore powder product with active ingredients and its preparation method | |
KR20150030012A (en) | High density manufacturing method of effective component from Ginsenosides and Product using the same | |
KR101095357B1 (en) | Processed Ginseng | |
KR101777673B1 (en) | Preparation method of ginsenoside-Rd using an enzyme | |
CN106723043A (en) | A kind of food compositions of three high drop | |
KR101224574B1 (en) | Manufacturing method of fermentative red ginseng | |
CN112457359A (en) | Method for preparing converted ginsenoside from ginseng fruit and preparation thereof | |
KR101233991B1 (en) | Manufacturing method of fermentative red ginseng | |
CN112898189B (en) | Method for preparing cucurbitacin from supercritical pumpkin seed protein treatment waste liquid | |
KR101465303B1 (en) | Method of Preparing Red Ginseng Concentrate Having Increased Active Ingredient | |
KR20130074118A (en) | Ginseng prosapogenin high concentration containing ginseng berry preparation using sonication and process for thereof | |
KR20130074120A (en) | Ginseng prosapogenin high concentration containing ginseng flower preparation using sonication and process for thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20141229 Year of fee payment: 4 |
|
FPAY | Annual fee payment |
Payment date: 20160628 Year of fee payment: 5 |
|
LAPS | Lapse due to unpaid annual fee |