KR20020028637A - Process for preparing ginkgo-tea and ginkgo-tea prepared thereby - Google Patents
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- 238000004519 manufacturing process Methods 0.000 title abstract description 8
- 235000008100 Ginkgo biloba Nutrition 0.000 claims abstract description 83
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 61
- 244000269722 Thea sinensis Species 0.000 claims abstract description 45
- 241000218628 Ginkgo Species 0.000 claims abstract description 37
- 235000011201 Ginkgo Nutrition 0.000 claims abstract description 37
- 229930002875 chlorophyll Natural products 0.000 claims abstract description 16
- 235000019804 chlorophyll Nutrition 0.000 claims abstract description 16
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 claims abstract description 16
- 239000012454 non-polar solvent Substances 0.000 claims abstract description 14
- 238000001035 drying Methods 0.000 claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000012046 mixed solvent Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 238000002156 mixing Methods 0.000 claims abstract description 9
- 150000002576 ketones Chemical class 0.000 claims abstract description 7
- 235000006468 Thea sinensis Nutrition 0.000 claims abstract description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 54
- 244000194101 Ginkgo biloba Species 0.000 claims description 46
- 239000002904 solvent Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 5
- 238000004821 distillation Methods 0.000 claims description 4
- 239000003208 petroleum Substances 0.000 claims description 3
- 238000000638 solvent extraction Methods 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000000284 extract Substances 0.000 abstract description 17
- 230000000144 pharmacologic effect Effects 0.000 abstract description 4
- 238000002360 preparation method Methods 0.000 abstract description 2
- 238000001704 evaporation Methods 0.000 abstract 1
- 239000000796 flavoring agent Substances 0.000 abstract 1
- 235000019634 flavors Nutrition 0.000 abstract 1
- 231100000956 nontoxicity Toxicity 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
- 235000013616 tea Nutrition 0.000 description 30
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 241000196324 Embryophyta Species 0.000 description 16
- 210000004027 cell Anatomy 0.000 description 12
- 238000000605 extraction Methods 0.000 description 11
- 239000003440 toxic substance Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 8
- 231100000614 poison Toxicity 0.000 description 8
- YXHVCZZLWZYHSA-FPLPWBNLSA-N Ginkgoic acid Chemical compound CCCCCC\C=C/CCCCCCCC1=CC=CC(O)=C1C(O)=O YXHVCZZLWZYHSA-FPLPWBNLSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 210000000170 cell membrane Anatomy 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 230000003204 osmotic effect Effects 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 230000017531 blood circulation Effects 0.000 description 4
- 229930003935 flavonoid Natural products 0.000 description 4
- 150000002215 flavonoids Chemical class 0.000 description 4
- 235000017173 flavonoids Nutrition 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000005292 vacuum distillation Methods 0.000 description 4
- YXHVCZZLWZYHSA-UHFFFAOYSA-N (Z)-6-[8-pentadecenyl]salicylic acid Natural products CCCCCCC=CCCCCCCCC1=CC=CC(O)=C1C(O)=O YXHVCZZLWZYHSA-UHFFFAOYSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 235000009569 green tea Nutrition 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000009429 Ginkgo biloba extract Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- MOLPUWBMSBJXER-YDGSQGCISA-N bilobalide Chemical compound O([C@H]1OC2=O)C(=O)[C@H](O)[C@@]11[C@@](C(C)(C)C)(O)C[C@H]3[C@@]21CC(=O)O3 MOLPUWBMSBJXER-YDGSQGCISA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000035622 drinking Effects 0.000 description 2
- 239000000469 ethanolic extract Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000401 methanolic extract Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
- 210000003934 vacuole Anatomy 0.000 description 2
- 235000009024 Ceanothus sanguineus Nutrition 0.000 description 1
- 229920002160 Celluloid Polymers 0.000 description 1
- 240000003553 Leptospermum scoparium Species 0.000 description 1
- 235000015459 Lycium barbarum Nutrition 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 235000020279 black tea Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000002481 ethanol extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229940068052 ginkgo biloba extract Drugs 0.000 description 1
- 235000020686 ginkgo biloba extract Nutrition 0.000 description 1
- YXHVCZZLWZYHSA-BQYQJAHWSA-N ginkgoic acid Chemical compound CCCCCC\C=C\CCCCCCCC1=CC=CC(O)=C1C(O)=O YXHVCZZLWZYHSA-BQYQJAHWSA-N 0.000 description 1
- FPUXKXIZEIDQKW-MFJLLLFKSA-N ginkgolide A Natural products O=C1[C@H](C)[C@@]2(O)[C@@H](O1)C[C@]13[C@@H]4OC(=O)[C@]21O[C@@H]1OC(=O)[C@H](O)[C@]31[C@@H](C(C)(C)C)C4 FPUXKXIZEIDQKW-MFJLLLFKSA-N 0.000 description 1
- 239000002035 hexane extract Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 210000004020 intracellular membrane Anatomy 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 239000002831 pharmacologic agent Substances 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/16—Tea extraction; Tea extracts; Treating tea extract; Making instant tea
- A23F3/18—Extraction of water soluble tea constituents
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/16—Tea extraction; Tea extracts; Treating tea extract; Making instant tea
- A23F3/22—Drying or concentrating tea extract
-
- 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
- A23V2250/214—Tea
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- 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)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
본 발명은 은행잎의 독성물질은 함유하지 않으면서 그의 유효성분은 그대로 함유하는 은행잎 차(ginkgo-tea)의 제조에 관한 것이다. 보다 구체적으로, 본 발명은 독성물질이 제거된 건조 은행잎에 그의 유효성분을 수용상태로 재이동시키고 건조시켜 은행잎 차를 제조하는 방법 및 그에 의해 제조된 은행잎 차에 관한 것이다.The present invention relates to the production of ginkgo-tea, which does not contain the toxic substance of ginkgo biloba, but contains its active ingredient as it is. More specifically, the present invention relates to a method for producing ginkgo biloba tea by removing and drying its active ingredient in a water-soluble state on dried ginkgo biloba leaves from which toxic substances have been removed, and the ginkgo biloba tea produced thereby.
은행잎이 함유하는 약리성분은 총 25 종 이상의 후라보노이드(flavonoid) 성분과 테르펜락톤(terpenelactone) 성분인 빌로발라이드(Bilobalide), 및 징콜라이드(Gingkolide) A, B, C, M 및 J이다. 이들 성분은 종합적으로 혈류를 촉진시키므로 혈류장애로부터 파생되는 일련의 질병을 예방 및 치료하는데 유효하다.The pharmacological components contained in ginkgo biloba are a total of 25 or more flavonoid components and terpenelactone components, bilobalide, and gingkolide A, B, C, M and J. These components promote comprehensive blood flow and are effective in preventing and treating a series of diseases derived from blood flow disorders.
본 발명에 포함되는 또 하나의 식물잎인 녹차의 주작용 천연물질은 후라보노이드 성분이며 이들 중에는 구조상 은행잎의 후라보노이드와 중첩되는 것도 있다. 따라서, 상기한 식물 잎에 은행잎 성분을 포함시키면 후라보노이드 성분이 보강되어 그 약효는 더욱 강화될 것이다.The main natural substance of green tea, which is another plant leaf included in the present invention, is a flavonoid component, and some of them overlap with flavonoids of ginkgo biloba. Therefore, the inclusion of ginkgo biloba leaves in the plant leaves will enhance the flavonoids components will further enhance their efficacy.
은행잎으로부터 혈류 촉진작용을 갖는 성분을 추출하여 제조된 여러 의약품이 개발되어 다양한 명칭으로 시판되고 있다. 그러나, 자연상태의 은행잎은 유효 약리 성분 이외에도 불필요한 성분들을 함유하고 있다. 특히, 은행잎은 차(茶)로 음용하기에는 적합하지 않는 맛과 냄새를 갖고 있을 뿐만 아니라 피부를 자극하는 징콜산(ginkgolic acid) 및 그의 유사체를 함유하고 있다. 따라서, 은행과육과 마찬가지로 은행잎에 함유되어 있는 이들 독성물질의 제거가 은행잎을 차로 이용하는데 있어서 가장 중요한 부분이 된다.Various medicines have been developed by extracting components having a blood flow promoting action from ginkgo biloba and have been marketed under various names. However, natural ginkgo leaves contain unnecessary ingredients in addition to the active pharmacological ingredients. In particular, ginkgo biloba leaves contain ginkgolic acid and the like, which not only have a taste and odor that are not suitable for drinking as tea, but also irritate the skin. Therefore, the removal of these toxic substances contained in ginkgo biloba leaves, like ginkgo pulp, is the most important part of using ginkgo biloba as tea.
일반적으로, 식물의 잎은 80% 이상의 수분을 함유하고 있으며 이 수분은 식물세포의 팽창성, 확산작용 및 삼투압에 의하여 세포내에서 항상적으로 유지된다. 팽창성은 식물세포의 젤라틴양 단백질, 점액질(mucilage), 셀룰로즈류(celluloid polymer), 전분류 등의 극성기, 예를들어 -COOH, -OH, -NH2, -CO- 등과 물분자가 결합하여 이들 고분자간의 거리를 증가시키는, 말하자면 용해현상을 가리킨다. 확산작용은 식물세포막 내외의 물질 농도가 다른 경우 물질 농도가 평형상태에 이르고자하는 성질을 의미한다. 그러나, 식물세포막은 선택성을 가지므로 세포막 안팎의 물질 농도가 상이한데 이 현상에 의해 삼투압이 생기게 된다.In general, the leaves of the plant contain more than 80% moisture, which is constantly maintained in the cell by the expansion, diffusion and osmotic pressure of the plant cells. The expandability is combined with water molecules such as gelatin-like proteins, mucilage, celluloid polymers, starch, etc. of plant cells, for example, -COOH, -OH, -NH 2 , -CO- It refers to the phenomenon of dissolution, which increases the distance between polymers. Diffusion refers to the nature of the concentration of the substance to reach the equilibrium when the substance concentration in the plant cell membrane is different. However, since plant cell membranes have selectivity, the concentrations of substances inside and outside the cell membranes are different, resulting in osmotic pressure.
식물을 건조시켜 탈수상태로 하면 식물세포는 흡습성으로 된다. 이때 식물세포중 액포(液胞; vacuole)내의 수분함량이 감소하고 고분자들간에 존재하는 수분량도 감소하여 고분자간의 거리가 가까워지므로 식물체의 크기 및 중량이 감소한다. 이렇게 건조된 잎세포의 액포내 물질들은 심하게 농축되어 물과 접촉시 강한 삼투압으로 물을 보충한다. 한편, 건조된 극성 폴리머들은 물과 결합하여 물로 둘러쌓인 형태의 복합물(micelle)을 형성하며, 이 복합물사이에 물분자가 끼어들어 결과적으로 세포는 팽창한다.When the plant is dried and dehydrated, the plant cells become hygroscopic. At this time, the water content in the vacuole of the plant cells decreases, and the water content present between the polymers decreases, thereby decreasing the size and weight of the plant as the distance between the polymers approaches. Substances in the vacuoles of the dried leaf cells are concentrated heavily to replenish water with strong osmotic pressure upon contact with water. Dried polar polymers, on the other hand, combine with water to form a composite surrounded by water, with water molecules between them, resulting in cell expansion.
이 흡습성은 잎을 건조시키는 방법에 따라 다른 양상을 띤다. 예를 들어, 어떤 잎을 진공을 사용하여 0℃ 내지 실온에서 건조시키면 식물세포의 생리기능이 거의 유지된다. 이렇게 건조된 잎을 물과 접촉시키면 물을 흡수하여 건조이전의 자연상태의 잎으로 되돌아간다. 그러나, 대부분의 차 제조과정에서는 차잎을 열을 가해 볶은후 음건 또는 열풍건조시킨다. 또한, 홍차를 제조하는 경우와 같이 차잎을 발효시키는 예도 있다. 열을 가하거나 발효시키면 대다수의 잎세포는 손상을 입어 물과 접촉시켜도 삼투압에 의한 팽창현상은 줄어든다.This hygroscopicity depends on the method of drying the leaves. For example, when certain leaves are dried at 0 ° C. to room temperature using a vacuum, the physiological function of the plant cells is almost maintained. When the dried leaves are brought into contact with water, they absorb the water and return to the natural leaves before drying. However, in most tea manufacturing processes, the tea leaves are heated and roasted to dry the shade or hot air. In addition, there is an example of fermenting tea leaves as in the case of manufacturing black tea. When heated or fermented, most leaf cells are damaged, and the contact with water reduces the expansion caused by osmotic pressure.
이상 식물잎과 물사이의 생리현상에 대해 기술하였다. 실제로 물은 물론 물에 용해되어 있는 모든 물질은 식물세포막을 통해 이동한다. 세포막의 선택성으로 인해 불필요한 물질의 세포내로의 이동이 제한된다. 그러나 잎을 약하게 볶거나 열을 가하여 건조시키면 대다수의 잎세포는 손상을 입게되어 세포의 원래기능이 소실된다. 특히 세포내막의 선택성이 손상을 입게되므로 삼투압 현상이 손상을 입는다. 이 경우 실제로 잎의 팽창요인중 용질의 확산과 탈수된 고분자와 결합하는 능력만 남는다.This has described the physiological phenomena between plant leaves and water. Indeed, all water dissolved in water, as well as water, travels through plant cell membranes. The selectivity of the cell membrane limits the movement of unwanted substances into the cells. However, if the leaves are lightly roasted or dried with heat, most of the leaf cells are damaged and their original function is lost. In particular, because the selectivity of the intracellular membrane is damaged, the osmotic phenomenon is damaged. In this case, only the diffusion of the solute and the ability to bind to the dehydrated polymer remain among the expansion factors of the leaves.
본 발명자들은 상기한 바와 같은 식물잎의 생리현상을 기초로 하여, 여러가지 수단으로 독성물질이 제거된 건조 은행잎을 제조한 후 상기 은행잎의 세포표면 또는 내부로 수용상태의 은행잎 성분을 재이동시키고 건조시킴으로써 은행잎의 독성물질은 제거되고 그의 유효성분들은 그대로 함유되어 차로 음용하기에 매우 적합한 은행잎 조성물을 제조하였다.Based on the physiological phenomena of plant leaves as described above, the present inventors prepare dried ginkgo biloba leaves from which toxic substances have been removed by various means, and then, by relocating and drying the ginkgo biloba component in a water-soluble state to the cell surface or inside of the ginkgo biloba leaves. Toxic substances of ginkgo biloba are removed and its active ingredients are contained as it is, making a ginkgo biloba composition suitable for drinking tea.
따라서, 본 발명의 목적은 은행잎의 독성물질을 함유하지 않으면서 그의 유효성분들을 함유하는 은행잎 차의 제조방법 및 그에 의해 제조된 은행잎 차를 제공하는 것이다.Accordingly, it is an object of the present invention to provide a method for producing ginkgo biloba tea containing its active ingredients without containing toxic substances of ginkgo biloba and ginkgo biloba tea produced thereby.
본 발명은 은행잎을 알콜, 케톤, 또는 그와 물의 혼합용매로 용매추출하고 남은 잔사를 건조시켜 얻은 은행잎 잔사(GL)와 상기 용매추출물을 비극성용매 또는 그와 물의 혼합용매로 재추출하고 증발시켜 얻은 수층(GF)을 혼화 및 건조시켜 은행잎 차를 제조하는 방법에 관한 것이다.The present invention obtained by re-extracting the ginkgo leaf residue (GL) and the solvent extract obtained by solvent extraction of the ginkgo biloba leaves with alcohol, ketone, or a mixed solvent of water and water and the solvent extract with a non-polar solvent or a mixed solvent of water and water and evaporated The present invention relates to a method for producing a ginkgo leaf tea by mixing and drying an aqueous layer (GF).
이때, 차나무(Thea sinensis) 잎을 비극성용매로 추출하여 얻은 클로로필(chlorophyll)을 추가로 혼화할 수 있다. 본 방법에서는 비극성용매로서 헥산, 석유에테르 또는 리그로인을 사용할 수 있다.At this time, the chlorophyll obtained by extracting the leaves of Thea sinensis with a non-polar solvent may be further mixed. In this method, hexane, petroleum ether or ligroin can be used as the nonpolar solvent.
차의 실제조제에 있어서 은행잎 잔사(GL)와 수층(GF)을 40∼70:10∼20(중량:부피)의 비율로 혼화하는 것이 바람직하다. 또한, 이 혼합물은 0℃∼실온에서 진공건조하는 것이 바람직하다. 차에 클로로필을 가하는 방법에 있어서는 비극성용매중의 클로로필 용액을 은행잎 잔사(GL) 및 수층(GF)(GF0인 경우에는 물을 첨가한다)의 혼합물에 대해 500∼1500rpm의 교반하에서 용매증류속도와 동일 속도로 가하는 것이 바람직하다.In the actual preparation of tea, it is preferable to mix the ginkgo leaf residue GL and the water layer GF at a ratio of 40 to 70:10 to 20 (weight: volume). Moreover, it is preferable to vacuum-dry this mixture at 0 degreeC-room temperature. In the method of adding chlorophyll to tea, the chlorophyll solution in a nonpolar solvent is equal to the solvent distillation rate under agitation at 500-1500 rpm for a mixture of ginkgo biloba residue (GL) and water layer (GF). It is preferable to add at a speed.
본 발명은 또한 은행잎을 알콜, 케톤, 또는 그와 물의 혼합용매로 용매추출하고 남은 잔사를 건조시켜 얻은 은행잎 잔사(GL)와 상기 용매추출물을 비극성용매 또는 그와 물의 혼합용매로 재추출하고 증발시켜 얻은 수층(GF)을 혼화하여 건조시킴으로써 제조되는 은행잎 차에 관한 것이다.The present invention also extracts ginkgo biloba leaves with alcohol, ketone, or a mixed solvent of water and water and dried the remaining residues, and re-extracts the ginkgo leaf residue (GL) and the solvent extract with a non-polar solvent or a mixed solvent of water and evaporates the same. It relates to a ginkgo leaf tea produced by mixing and drying the obtained water layer (GF).
본 발명에 따른 은행잎 차는 차나무 잎을 비극성용매로 추출하여 얻은 클로로필을 추가로 혼화하여 제조될 수 있다. 여기에서, 은행잎 잔사(GL)의 수분함량은 5% 이하이고 최종산물인 은행잎 차의 수분함량은 10% 이하인 것이 바람직하다.Ginkgo biloba tea according to the present invention may be prepared by further mixing chlorophyll obtained by extracting the tea leaf with a non-polar solvent. Here, the water content of the ginkgo leaf residue (GL) is preferably 5% or less and the water content of the final product of the ginkgo leaf tea is 10% or less.
이하, 본 발명을 보다 상세히 설명한다.Hereinafter, the present invention will be described in more detail.
상기한 바와 같이, 자연상태의 은행잎은 혈류 촉진작용을 갖는 약리성분이외에 불필요한 성분들(피부자극성 징콜산 또는 그 유사체 등)을 함유하고 있으므로, 은행잎을 차로 이용하는데 있어서 이들 독성물질의 제거가 관건이 된다. 이들 독성물질은 고형물질이며 그 비점이 높아 증류방법으로 제거하기는 곤란하므로 본 발명자들은 이들을 추출에 의해 제거하는 것이 가장 바람직할 것으로 판단하였다. 또한, 은행잎 추출용매의 선택시 유의할 점은 세포내의 전분 및 그 분해산물이 용출되어 유실되지 않도록 하여야 한다는 점이다. 건조상태의 전분은 후술하는 유효성분의 재흡수에 중요한 역할을 하기 때문이다. 결과적으로 추출효율이나 가격면에서 알콜류 또는 케톤류, 예를들어, 아세톤, 메탄올, 에탄올 등, 또는 그들과 물의 혼합용매가 가장 적합한 추출용매임이 밝혀졌다. 이들은 은행잎의 유효성분은 물론 독성물질인 징콜산 및 그 유사체들도 동시에 용출시킨다.As mentioned above, ginkgo biloba in the natural state contains components other than pharmacological agents that promote blood flow, such as skin irritant ginkgolic acid or the like. Therefore, it is important to remove these toxic substances when using ginkgo biloba as a tea. do. Since these toxic substances are solid substances and their boiling points are high and difficult to remove by distillation, the inventors determined that it would be most preferable to remove them by extraction. In addition, when selecting the ginkgo biloba extract solvent, it is important that the starch and its degradation products in the cell should not be eluted and lost. This is because the dried starch plays an important role in resorption of the active ingredient described later. As a result, it was found that alcohols or ketones such as acetone, methanol, ethanol, or a mixed solvent of them and water were the most suitable extraction solvents in terms of extraction efficiency and price. They elute not only the active ingredient of ginkgo biloba, but also the toxic substance ginkgolic acid and its analogs.
본 발명의 추출절차를 간략히 기술하면 다음과 같다.Briefly describing the extraction procedure of the present invention.
알콜류, 케톤류 또는 이들과 물의 혼합용매중 한 가지를 택하여 은행잎을 추출한다. 추출 후 얻은 은행잎 잔사를 진공건조기에 가하고 건조시켜 수분함량 5% 이하의 건조된 은행잎 잔사(GL)를 제조하여 보관한다. 한편, 용매추출물을 비극성용매 또는 그와 물의 혼합용매로 재추출하여 징콜산 및 그 유사체(GH)를 제거한다. 이때 비극성용매로는 헥산, 석유에테르, 리그로인 등, 바람직하게는 헥산을 사용할 수 있다. 비극성용매로의 추출후 남은 수층이 활성엑기스(GF)이다. 일정량의 GF에 탈수된 GL을 가하고 철저히 혼합한 후 이 혼합물을 진공건조기에서 수분함량 10% 이하로 건조하여 은행잎 차를 제조한다.Ginkgo biloba is extracted by selecting one of alcohols, ketones, or a mixed solvent of these and water. Ginkgo leaf residue obtained after extraction is added to a vacuum dryer and dried to produce dried Ginkgo leaf residue (GL) having a moisture content of 5% or less and stored. Meanwhile, the solvent extract is reextracted with a nonpolar solvent or a mixed solvent of water and water to remove the zinc glycol acid and its analogue (GH). In this case, as the nonpolar solvent, hexane, petroleum ether, ligroin, and the like, preferably hexane can be used. The remaining water layer after extraction with the nonpolar solvent is the active extract (GF). Dehydrated GL was added to a certain amount of GF, mixed thoroughly, and the mixture was dried to 10% or less of moisture in a vacuum dryer to prepare ginkgo leaf tea.
본 발명의 구체적인 예를 들어보면 다음과 같다.Specific examples of the present invention are as follows.
은행잎 잔사(GL)에 대한 은행잎 유효성분의 재흡수Resorption of Ginkgo Biloba Active Ingredients from Ginkgo Leaf Residues (GL)
은행잎 100 g과 60% 아세톤 500 ㎖를 2000 ㎖ 추출기에 가하고 5∼10 시간동안 추출한다. 여과후 남은 은행잎 잔사에 다시 60% 아세톤 500 ㎖를 가하여 동일한 조건으로 추출한다. 여과후 남은 은행잎 잔사를 진공건조기에서 건조하여 수분함량 5% 이하가 되도록 건조하고 보관한다(GL). 이때 GL의 중량은 40∼70 g 범위이다.100 g of ginkgo biloba leaves and 500 ml of 60% acetone are added to a 2000 ml extractor and extracted for 5-10 hours. After filtration, 500 ml of 60% acetone was added to the remaining ginkgo biloba residues and extracted under the same conditions. The remaining ginkgo biloba residue after filtration was dried in a vacuum dryer and dried to be kept at 5% or less of moisture (GL). The weight of GL is in the range of 40 to 70 g.
회전식 감압증류기에서 60% 아세톤 추출물로부터 아세톤을 증발 제거한다. 남은 수층을 헥산 400 ㎖씩으로 3 회 추출한다. 남아있는 수층(GF)으로부터 물을 증발시켜 30 ㎖(GF30)가 되게 한다.Acetone is evaporated off from 60% acetone extract in a rotary vacuum distillation unit. The remaining aqueous layer is extracted three times with 400 ml each of hexane. Water is evaporated from the remaining aqueous layer (GF) to 30 ml (GF30).
동일한 방법으로 추출하여 최종추출물의 양이 20 ㎖(GF20), 10 ㎖(GF10), 5 ㎖(GF5) 및 건고물(GF0)이 되도록 한다. 각각의 GF 추출물들(GF0인 경우에는 다시금 물을 첨가한다)을 각 배치에서 얻은 GL과 20∼60 분간 혼화한후 진공건조기에가하고 건조하여 녹차로 제조한다.Extract in the same way to make the final extract 20 mL (GF20), 10 mL (GF10), 5 mL (GF5) and dry matter (GF0). Each GF extract (if GF0 is added again) is mixed with GL obtained in each batch for 20 to 60 minutes, then added to a vacuum dryer and dried to prepare green tea.
제조한 녹차 (건조물) 1 g을 물 80 ㎖에 가하고 80 ℃로 가온한 후 그 탁도를 관찰하였다. GF의 각 농도중 GF20과 GF10에서 가장 양호한 탁도를 얻을 수 있었고 GF30 및 GF5에서는 다소의 혼탁이 관찰되었다. 맛은 은행잎 엑기스의 전형적인 맛(약간 쓰면서 고소한 맛)을 나타내었다.1 g of the prepared green tea (dried) was added to 80 ml of water, warmed to 80 ° C, and the turbidity thereof was observed. Among the concentrations of GF, the best turbidity was obtained in GF20 and GF10, and some turbidity was observed in GF30 and GF5. The taste was typical of ginkgo leaf extract (slightly bitter).
은행잎 잔사(GL)에 대한 유효성분(GF) 및 클로로필의 재흡수Resorption of GF and Chlorophyll on Ginkgo Leaf Residue (GL)
건조시킨 차나무(Thea sinensis)의 어린잎을 헥산으로 추출하여 클로로필을 얻고(TH), 이를 GF와 함께 GL에 흡착시키는 조작이다. 이 조작의 목적은 은행잎 차로 하여금 클로로필의 맛과 색조를 띠게하는 것이다. GL에 클로로필과 GF를 가하여 혼합하는 과정에서는 클로로필의 분산상태가 매우 중요하다. 클로로필이 세밀하게 분산될수록 클로로필의 흡착이 더욱 균일해질 뿐 아니라 GF의 흡착도 잘 일어날 것이다. 이때 물은 혼합을 촉진하는 역할을 수행하므로 GF0(건고물)을 사용하는 경우에는 추가로 물을 첨가한다. 또한, 물에서 클로로필이 균일하게 분산되기 위해서는 물에 부분적으로 용해되는 용매의 존재가 중요하다. 이때 사용할 수 있는 용매로는 부탄올, 에틸아세테이트, 부탄온 등이 있다.The young leaves of dried Tea Tree ( Thea sinensis ) are extracted with hexane to obtain chlorophyll (TH), which is adsorbed with GL on GL. The purpose of this operation is to make ginkgo biloba tea taste and taste of chlorophyll. In the process of adding chlorophyll and GF to GL, the dispersion state of chlorophyll is very important. The finer the chlorophyll dispersion, the more uniform the chlorophyll adsorption and the better the adsorption of GF. At this time, since water plays a role of promoting mixing, additional water is added when using GF0 (dry). In addition, the presence of a solvent partially dissolved in water is important for the chlorophyll to be uniformly dispersed in water. At this time, the solvent may be used butanol, ethyl acetate, butanone.
이들 용매중 하나에 절반량의 TH를 용해시킨후 이를 GL 및 GF의 혼합물에 가한다. 이때 중요한 것은 혼합물의 교반속도와 TH의 첨가속도인데, 예를들어 GL 및 GF 일정량을 감압증류 장치가 부착된 교반기에 가하고 500∼1500 rpm의 회전속도로 교반하면서 TH 용액을 혼합물의 중간을 통하여 가한다. 이론적으로 TH 용액의 첨가속도는 용매 증류속도와 동일한 것이 좋고, 일반적으로 TH 용액 50 ㎖를 가하는데 소요되는 시간은 5∼30 분이다. 이렇게 하여 제조된 은행잎 차 중에는 은행잎이 함유한 원래의 유효성분이 그대로 함유되어있다.Half of TH is dissolved in one of these solvents and then added to a mixture of GL and GF. Important here is the stirring speed of the mixture and the addition speed of TH. For example, a certain amount of GL and GF is added to a stirrer equipped with a vacuum distillation unit and the TH solution is added through the middle of the mixture while stirring at a rotational speed of 500 to 1500 rpm. do. Theoretically, the addition rate of the TH solution is preferably the same as the solvent distillation rate, and generally, the time required to add 50 ml of the TH solution is 5 to 30 minutes. The ginkgo biloba tea produced in this way contains the original active ingredient contained in the ginkgo biloba.
[실험 1][Experiment 1]
유효성분의 정량법- 의약품등 기준 및 시험방법 제2개정 제1286면 <은행잎 엑스> 참조Determination of Active Ingredients-Standards and Test Methods, etc. of the 2nd Amendment, page 1286 <Ginkgo Leaf X>
은행잎차 1g에 함유되어 있는 징코푸라본의 평균함량은 3.6 mg이었다. The average content of ginkgo furabon in 1 g of ginkgo leaf tea was 3.6 mg .
[실험 2][Experiment 2]
은행잎차 중의 징콜산의 정량Determination of Jingkolic Acid in Ginkgo Leaf Tea
Sullivan 등의 HPLC 방법[참조: Sullivan.J.T.; Richards.C.S.; LIoyd.H.A.; Krishna.G: Planta Med. 44, 175 (1982)]에 따라 은행잎중의 징콜산 유도체 중 가장 많이 함유되어 있는 2-하이드록시-6-(8-펜타데세닐)벤조산(ginkgoic acid)을 정량하였던 바, 5g의 은행잎차중 이 산이 전혀 검출되지 않았다.HPLC methods of Sullivan et al. [Sullivan. J. T .; Richards. C. S .; LIoyd.H.A .; Krishna.G: Planta Med. 44, 175 (1982)] quantified 2-hydroxy-6- (8-pentadecenyl) benzoic acid (ginkgoic acid), which contains the most of ginkgolic acid derivatives in ginkgo biloba leaves. This acid was not detected at all.
[실시예]EXAMPLE
이하 본 발명을 실시예에 의해 구체적으로 설명하지만, 이에 의해 본 발명의 범위가 어떤 식으로든 제한되는 것은 아니다.Hereinafter, the present invention will be described in detail by way of examples, but the scope of the present invention is not limited in any way.
[실시예 1]Example 1
음건한 은행잎 100 g을 취하여 교반장치가 부착된 1000 ㎖ 추출기에 넣고 300 ㎖의 60% 아세톤을 가하여 10 시간동안 실온에서 추출하였다. 추출후 용매추출액을 분리 보관하고 은행잎 잔사에 다시 동일한 용매 300 ㎖씩으로 2 회 추출하여 추출액을 합하였다. 남아있는 은행잎 잔사를 진공건조기에서 건조하여 수분함량이 5% 이하인 은행잎을 얻었다(GL). 이때 건조된 은행잎(GL)의 양은 사용한 은행잎의 상태에 따라서 40∼70 g이었다. 이를 방습이 잘되는 용기에 보관하였다. 60% 아세톤 추출물을 감압증류기에서 증류하여 아세톤을 완전히 제거하였다. 이때 남아있는 수층을 헥산 100 ㎖씩으로 3 회 추출하였다. 헥산 추출후 남아있는 수층(GF)으로부터 물을 증발시키고 20 ㎖의 농축액(GF20)을 얻었다. 헥산 용해부분은 폐기하였다.100 g of dried ginkgo biloba leaves were taken into a 1000 ml extractor equipped with a stirring device, and 300 ml of 60% acetone was added thereto, followed by extraction at room temperature for 10 hours. After extraction, the solvent extract was separated and stored, and the extract was extracted twice with 300 ml of the same solvent to the ginkgo leaf residue, and the extracts were combined. The remaining ginkgo leaf residue was dried in a vacuum dryer to obtain a ginkgo leaf having a moisture content of 5% or less (GL). At this time, the amount of dried ginkgo leaves (GL) was 40 to 70 g depending on the state of the ginkgo leaves used. It was stored in a moisture-proof container. 60% acetone extract was distilled in a vacuum distillation to completely remove acetone. At this time, the remaining aqueous layer was extracted three times with 100 ml of hexane. Water was evaporated from the remaining aqueous layer (GF) after hexane extraction and 20 ml of concentrate (GF20) was obtained. The hexane dissolved portion was discarded.
[실시예 2]Example 2
실시예 1과 동일한 방법으로 GF를 얻고 물을 증발시켜 10 ㎖가 되게 하였다(GF10).GF was obtained in the same manner as in Example 1, and water was evaporated to 10 ml (GF10).
[실시예 3]Example 3
실시예 1에서 얻은 GL 전량에 실시예 1에서 얻은 GF20을 가하고 잘 버무린후 건조기에 가하고 건조하여 수분함량 10%인 은행잎 차를 얻었다. 1 회 용량 1 g 씩 포장하였다.To the total amount of GL obtained in Example 1, GF20 obtained in Example 1 was added, mixed well, and added to a drier, followed by drying to obtain a ginkgo leaf tea having a water content of 10%. 1 g each was dosed.
[실시예 4]Example 4
실시예 1에서 얻은 GL 전량에 실시예 2에서 얻은 GF10을 가하고 잘 버무린후 건조기에 가하고 건조하여 수분함량 5% 이하인 차를 얻었다. 1 회 용량 1 g 씩 포장하였다.To the total amount of GL obtained in Example 1, GF10 obtained in Example 2 was added, mixed well, and added to a drier, followed by drying to obtain a tea having a water content of 5% or less. 1 g each was dosed.
[실시예 5]Example 5
음건한 은행잎을 30∼50 메쉬로 세절하고 이중 100 g을 취하여 1000 ㎖의 추출기에 넣었다. 여기에 메탄올 300 ㎖를 가하고 5∼10 시간동안 실온에서 추출하였다. 추출후 여과하여 은행잎 잔사와 메탄올 추출물로 나누었다. 은행잎 잔사에 대해 동일한 조작을 2 회 더 반복하였다. 여과하고 남은 은행잎 잔사를 진공건조기에 가하고 건조하여 수분함량 5% 이하로 만들었다(GLm). 메탄올 추출물을 합하고 감압하에서 용매를 증발시켰다. 이 잔류물에 물 40∼50 ㎖를 가하고 헥산 100 ㎖를 가한후 30 분간 진탕하였다. 10 분간 방치한후 수층과 헥산층을 분리하였다. 하부의 수층에 대해서는 2 회 더 동일한 조작을 행하였다. 헥산 추출후 남아있는 수층(GFm)을 20 ㎖로 농축하였다(GFm20). 헥산층은 폐기하였다.The dried ginkgo biloba was cut into 30-50 meshes, 100 g of which were placed in a 1000 ml extractor. To this was added 300 ml of methanol and extracted at room temperature for 5-10 hours. After extraction, the resultant was filtered and divided into a ginkgo leaf residue and a methanol extract. The same operation was repeated two more times for the ginkgo leaf residue. The remaining ginkgo leaf residue after filtration was added to a vacuum dryer and dried to obtain a water content of 5% or less (GLm). The methanol extracts were combined and the solvent was evaporated under reduced pressure. 40-50 mL of water was added to this residue, followed by shaking for 30 minutes after adding 100 mL of hexane. After standing for 10 minutes, the aqueous and hexane layers were separated. The same operation was performed twice about the lower water layer. The remaining aqueous layer (GFm) after hexane extraction was concentrated to 20 mL (GFm20). The hexane layer was discarded.
[실시예 6]Example 6
실시에 5와 동일한 방법으로 GFm을 얻고 물을 증발시켜 10 ㎖가 되게 하였다(GFm10).GFm was obtained in the same manner as in Example 5, and water was evaporated to 10 ml (GFm10).
[실시예 7]Example 7
GFm20과 GLm을 혼합하고 건조하여 수분함량이 10% 이하인 차를 제조하였다. 1 회 용량 1 g 씩 포장하였다.GFm20 and GLm were mixed and dried to prepare a tea having a water content of 10% or less. 1 g each was dosed.
[실시예 8]Example 8
GFm10과 GLm을 혼합하고 건조하여 수분함량이 5% 이하인 차를 제조하였다. 1회 용량은 1 g으로 하였다.GFm10 and GLm were mixed and dried to prepare tea with a moisture content of 5% or less. One dose was 1 g.
[실시예 9]Example 9
음건한 은행잎을 30∼50 메쉬로 세절하고 이중 100 g을 취하여 1000 ㎖의 추출기에 넣고 에탄올 300 ㎖를 가한후 실온에서 5∼10 시간동안 교반하였다. 에탄올 추출액을 여과하여 보관하고 은행잎 잔사에 대하여 동일한 조작을 2 회 더 실시하였다. 에탄올 추출후 남은 은행잎 잔사는 진공건조기에서 건조하여 수분함량 5% 이하가 되게 한 후 밀폐용기에 보관하였다(GLe). 에탄올 추출물은 합한후 감압 증류기에서 에탄올을 제거하여 잔사를 얻었다. 이 잔사에 물 30∼50 ㎖를 가한후 헥산 200 ㎖를 가하고 실온에서 30∼60 분간 진탕한후 헥산층과 수층을 분리하였다. 수층에 대해서는 동일한 조작을 2 회 더 반복하였다. 수층을 취하고 농축하여 20 ㎖가 되게 하고(GFe20) 헥산층은 폐기하였다.Dried ginkgo biloba leaves were cut into 30-50 meshes, 100 g of which were added to a 1000 ml extractor, and 300 ml of ethanol were added, followed by stirring at room temperature for 5 to 10 hours. The ethanol extract was stored by filtration and the same operation was performed twice on the ginkgo leaf residue. Ginkgo leaf residue after ethanol extraction was dried in a vacuum dryer to less than 5% moisture content and stored in a sealed container (GLe). The ethanol extracts were combined and ethanol was removed in a reduced pressure distiller to obtain a residue. After adding 30-50 mL of water to this residue, 200 mL of hexane was added, followed by shaking at room temperature for 30 to 60 minutes, and the hexane layer and the aqueous layer were separated. For the aqueous layer, the same operation was repeated two more times. The aqueous layer was taken and concentrated to 20 mL (GFe20) and the hexane layer was discarded.
상기 실시예 전과정을 2 회 반복하여 수층을 얻고 농축하여 각각 10 ㎖(GFe10)와 건고물(GFe0)을 얻었다.The entire procedure of the above example was repeated twice to obtain an aqueous layer and concentrated to obtain 10 ml (GFe10) and dried product (GFe0), respectively.
[실시예 10]Example 10
GFe20과 GLe을 혼합한후 버무리고 감압건조하여 수분함량 10% 이하의 차를 제조하였다. 1 회 용량을 1 g으로 하였다.After mixing GFe20 and GLe, tossed and dried under reduced pressure, a tea having a water content of 10% or less was prepared. One dose was 1 g.
[실시예 11]Example 11
GFe10과 GLe을 혼합한후 버무리고 감압건조하여 수분함량 5% 이하의 차를 제조하였다. 1 회 용량을 1 g으로 하였다.After mixing GFe10 and GLe, tossed and dried under reduced pressure, a tea having a water content of 5% or less was prepared. One dose was 1 g.
[실시예 12]Example 12
차나무의 어린 잎을 음건한 후 이중 100 g을 취하여 추출기에 가하였다. 여기에 헥산 300 ㎖를 가하고 실온에서 1∼3 시간동안 교반하였다. 여과한후 헥산 추출물은 보관하고 남은 식물체에 대하여 동일한 조작을 2 회 더 반복하였다. 헥산층을 합하고 농축하여 녹색 잔사를 얻었다. 얻은 잔사의 절반을 덜어서 에틸아세테이트 50 ㎖에 용해시켰다(TH50).After drying the young leaves of the tea tree, 100 g of these were added to the extractor. To this was added 300 ml of hexane and stirred at room temperature for 1-3 hours. After filtering, the hexane extract was stored and the same operation was repeated twice more for the remaining plants. The hexane layers were combined and concentrated to give a green residue. Half of the obtained residue was dissolved in 50 ml of ethyl acetate (TH50).
한 배취의 GLm(또는 GLe) 50 g, GFm0(또는 GFe0) 및 증류수 50∼70 ㎖를 500 ㎖ 크기의 감압증류 장치가 부착된 교반기, 예를들어 회전식 감압증류기에 가하고 500∼1000 rpm의 속도로 회전시켰다. 용매 주입 튜브를 통하여 TH50을 소량씩 혼합물의 중간지점에 흘려보냈다. 흘려보내는 속도를 분당 5 ㎖ 정도로 하면 분당 5 ㎖ 정도의 에틸아세테이트가 증발하도록 조절하였다. 첨가시간은 10∼20 분이었다. TH50의 첨가가 완결되면 물을 증발시켜 초벌 건고물을 제조하였다. 초벌 건고물은 감압건조하여 수분함량 10% 이하인 차를 만들었다. 1 회 용량 1 g 씩 포장하였다.50 g of GLm (or GLe), GFm0 (or GFe0) and 50 to 70 ml of distilled water are added to a stirrer equipped with a 500 ml vacuum distillation unit, for example a rotary vacuum distiller, at a speed of 500 to 1000 rpm. Rotated. A small amount of TH50 was flown through the solvent injection tube to the midpoint of the mixture. When the flow rate was about 5 ml per minute, it was adjusted to evaporate about 5 ml per minute of ethyl acetate. The addition time was 10-20 minutes. When the addition of TH50 was completed, water was evaporated to prepare a dry dry matter. The dried product was dried under reduced pressure to make tea with 10% or less moisture. 1 g each was dosed.
본 발명에 따르면 은행잎의 독성물질은 함유하지 않으면서 그의 약리효과 및 은행잎 고유의 맛과 향을 그대로 즐길 수 있는 은행잎 차를 제조할 수 있다.According to the present invention can be produced without toxic substances of ginkgo biloba leaves ginkgo biloba tea can enjoy its pharmacological effects and the unique taste and aroma of ginkgo biloba as it is.
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KR101032459B1 (en) * | 2011-01-20 | 2011-05-03 | (주)보성녹차테크 | How to prepare high quality chlorophyll extract |
KR20190046365A (en) * | 2017-10-26 | 2019-05-07 | 주식회사 보락 | Method for preparing excipient for tableting comprising green tea residue and method for preparing green tea tablet using the same |
CN116530590A (en) * | 2023-05-06 | 2023-08-04 | 安徽农业大学 | A tea processing method that greatly increases the content of kaempferol and reduces the bitterness and astringency |
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JPH0724560B2 (en) * | 1990-06-01 | 1995-03-22 | 株式会社ヤクルト本社 | Beverage containing plant extract |
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KR101032459B1 (en) * | 2011-01-20 | 2011-05-03 | (주)보성녹차테크 | How to prepare high quality chlorophyll extract |
KR20190046365A (en) * | 2017-10-26 | 2019-05-07 | 주식회사 보락 | Method for preparing excipient for tableting comprising green tea residue and method for preparing green tea tablet using the same |
CN116530590A (en) * | 2023-05-06 | 2023-08-04 | 安徽农业大学 | A tea processing method that greatly increases the content of kaempferol and reduces the bitterness and astringency |
CN116530590B (en) * | 2023-05-06 | 2023-11-28 | 安徽农业大学 | Tea processing method capable of greatly improving kaempferol content and reducing bitter taste |
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