JPS63201108A - Production of water-soluble extract extracted from flower or seed of safflower - Google Patents
Production of water-soluble extract extracted from flower or seed of safflowerInfo
- Publication number
- JPS63201108A JPS63201108A JP62031968A JP3196887A JPS63201108A JP S63201108 A JPS63201108 A JP S63201108A JP 62031968 A JP62031968 A JP 62031968A JP 3196887 A JP3196887 A JP 3196887A JP S63201108 A JPS63201108 A JP S63201108A
- Authority
- JP
- Japan
- Prior art keywords
- safflower
- extract
- extraction
- flower
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 244000020518 Carthamus tinctorius Species 0.000 title claims abstract description 29
- 235000003255 Carthamus tinctorius Nutrition 0.000 title claims abstract description 29
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 239000000284 extract Substances 0.000 title abstract description 51
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims abstract description 16
- 239000000049 pigment Substances 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 229940119485 safflower extract Drugs 0.000 claims abstract description 9
- 235000019485 Safflower oil Nutrition 0.000 claims abstract description 5
- 235000005713 safflower oil Nutrition 0.000 claims abstract description 5
- 239000003813 safflower oil Substances 0.000 claims abstract description 5
- 238000000354 decomposition reaction Methods 0.000 claims description 15
- 238000000855 fermentation Methods 0.000 claims description 4
- 230000004151 fermentation Effects 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 abstract description 12
- 108090000790 Enzymes Proteins 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 12
- 239000003814 drug Substances 0.000 abstract description 10
- 238000000605 extraction Methods 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 7
- 229940079593 drug Drugs 0.000 abstract description 7
- 102000003425 Tyrosinase Human genes 0.000 abstract description 6
- 108060008724 Tyrosinase Proteins 0.000 abstract description 6
- 239000003513 alkali Substances 0.000 abstract description 6
- 230000002401 inhibitory effect Effects 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 3
- 239000002994 raw material Substances 0.000 abstract description 3
- 230000001256 tonic effect Effects 0.000 abstract description 2
- 235000013402 health food Nutrition 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229940088598 enzyme Drugs 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000002537 cosmetic Substances 0.000 description 8
- 230000002255 enzymatic effect Effects 0.000 description 7
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229940024606 amino acid Drugs 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- -1 Polyoxyethylene lauryl ether Polymers 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 230000003020 moisturizing effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229960004441 tyrosine Drugs 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- 240000005220 Bischofia javanica Species 0.000 description 1
- 235000010893 Bischofia javanica Nutrition 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 108010059820 Polygalacturonase Proteins 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 210000001557 animal structure Anatomy 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000006862 enzymatic digestion Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 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
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9728—Fungi, e.g. yeasts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/74—Biological properties of particular ingredients
- A61K2800/78—Enzyme modulators, e.g. Enzyme agonists
- A61K2800/782—Enzyme inhibitors; Enzyme antagonists
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/005—Preparations for sensitive skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)発明の目的
本発明は、新規なベニバナの花又は種子を用いて得られ
る水溶性抽出エキス(以下、単にベニバナ抽出エキスと
1便宜上述べる。)の製造法に関するものである。Detailed Description of the Invention (a) Purpose of the Invention The present invention relates to a method for producing a water-soluble extract obtained using novel safflower flowers or seeds (hereinafter simply referred to as safflower extract for convenience). It is something.
(産業上の利用分野)
本発明による方法で得られたベニバナ抽出エキスは、化
粧品を始め、医薬部外品、医薬品、飲料等に用いること
が出来る。(Field of Industrial Application) The safflower extract obtained by the method of the present invention can be used in cosmetics, quasi-drugs, pharmaceuticals, drinks, etc.
又1本法に採用した抽出処理法によれば、ベニバナの他
、各種の薬用植物からエキスを抽出するに利用出来る。Also, according to the extraction treatment method adopted in this method, it can be used to extract extracts from various medicinal plants in addition to safflower.
(従来の技術)
ベニバナは、花、及び種子をもとに利用されており、花
からは色素(染料)が油出され、その圧搾後の残渣物に
相当するものを、漢方では、(日周収載名称)紅花(コ
ウカ)と称し、古くから。(Prior art) Safflower is used based on its flowers and seeds. Pigments (dyes) are extracted from the flowers, and in Chinese medicine, the residue after pressing is Since ancient times, it has been called safflower.
医薬品(内層、外用)剤、化粧品などに用いられてきて
いる。又、得られた色素は、化粧品、染料として用いら
れてきている。さらに種子からは。It has been used in pharmaceuticals (inner layer and external use), cosmetics, etc. In addition, the obtained pigments have been used as cosmetics and dyes. Furthermore, from seeds.
ベニバナ油が抽出されて、有効利用されている。Safflower oil is extracted and put to effective use.
(発明が解決しようとする問題点)
従来、ベニバナの花からは1色素を抽出し、又ベニバナ
の種子から油を抽出していた。しかし。(Problems to be Solved by the Invention) Conventionally, one pigment was extracted from safflower flowers, and oil was extracted from safflower seeds. but.
花から色素を抽出したものは1日局てはコウカと呼ばれ
、又、板紅花とも呼び、漢方薬の処方中に用いられるに
すぎなかった0本発明で用いる原料は、このいわば、ベ
ニバナの花から色素を除去した残渣物、さらに、ベニバ
ナの種子から油を抽出した後の残渣物をもとに、化粧品
に有益hエキスを得ることにある。The pigment extracted from the flower is called safflower, and is also called safflower, and is only used in the prescription of Chinese herbal medicine.The raw material used in the present invention is the so-called safflower flower. To obtain an H extract useful for cosmetics based on a residue obtained by removing pigments from safflower seeds and a residue obtained after extracting oil from safflower seeds.
すなわち、従来は、これらのベニバナ由来の残wi物は
、特に利用されることもなく、その有効利用が望まれて
いたのである。That is, in the past, these safflower-derived residues were not particularly utilized, and their effective utilization was desired.
そこで、本発明者らは、使用されずにいた。いわゆる、
抽出後のカスの部分のついて、有効利用することを、研
究開発のテーマとして、その応用に当った。Therefore, the inventors remained unused. So-called,
The research and development theme was to effectively utilize the residue after extraction.
但し、すでに1日局に収載されるコウカからは、これを
乾燥、粉砕して、##機溶媒、酵素、酸やアルカリを作
用させて得られた抽出エキスは。However, the extract obtained from Kouka, which has already been listed on the 1st Bureau, is obtained by drying, pulverizing, and reacting with organic solvent, enzyme, acid, or alkali.
すでに開発されている。しかし、独特な異臭を生じたり
することb(あり1例えば、化粧品などに用いるに当っ
ては、その異臭を除去するなどの改善策が求められてい
た。Already developed. However, it may produce a unique off-odor (1) For example, when used in cosmetics, there has been a need for improvement measures such as removing the off-odor.
(ロ)発明の4IdL 本発明に用いる原料は。(b) 4IdL of invention Raw materials used in the present invention.
(1) ベニバナの花期の管状化より色素を抽出した
際の残渣物。(1) Residue from extracting pigment from tubular safflower during flowering stage.
(2) ベニバナの種子より、サフラワー油を抽出した
際の残渣物を出発原料となし、酸やアルカリ分解、又は
酵素分解して得られた分解液を、さらに、酵母を添加し
て1発酵させて得られることを特徴とするベニバナ抽出
エキスの製造法からなる。(2) Using the residue from extracting safflower oil from safflower seeds as a starting material, the decomposed liquid obtained by acid or alkali decomposition or enzymatic decomposition is further added to yeast for one fermentation. This method consists of a method for producing a safflower extract, which is characterized in that it can be obtained by
具体的には、以下に詳記するも、上記で特定したa料は
、以下、単にM料(1)〜(2)で示す。Although specifically detailed below, the A materials specified above will be simply referred to as M materials (1) and (2) below.
(問題を解決するための手段)
「実施例!」
前記、発明の構成で記載した。ベニバナ由来の原ネ4(
1)〜(2)の内、その1つ、又は、両方を混合したも
のに、酸やアルカリ分解を加えるか、酵素(セルラーゼ
、ペクチナーゼなど)を胎えて反応させ、加水分解を行
い、(この際の反応系中の至適pHは、使用する鑓やア
ルカリの組み合わせ、あるいは、用いる酵素によって違
いがあるが、常法(公知)な手法を用い、至適pHに調
整した上て行う、)
例えば、酵素分解条件としては、lo〜70’C(至適
温度:30〜50”C)、0.5〜24時間(至適時間
:2〜6時間)で反応させることにより、十分な酵素分
解液が出来る。(Means for solving the problem) "Example!" The configuration of the invention has been described above. Raw energy derived from safflower 4 (
1) to (2), one or both of them can be hydrolyzed by adding acid or alkaline decomposition, or reacting with enzymes (cellulase, pectinase, etc.). The optimum pH in the reaction system differs depending on the combination of alkali and alkali used, or the enzyme used, but it is carried out after adjusting to the optimum pH using a conventional (known) method.) For example, as the enzymatic decomposition conditions, sufficient enzymes can be A decomposition liquid is produced.
得られた分解液は、加熱処理を行い、酵素を用いた場合
ては、酵素の失活を行つた後、又、酸やアルカリを用い
た分解液では、中和した後、酵母を1体重量(ペースト
状)で1分解液に対して。The obtained decomposition solution is heat-treated to deactivate the enzyme if an enzyme is used, or after neutralization in the case of an acid or alkali decomposition solution, one yeast is removed. Weight (paste) per 1 decomposition solution.
O11〜5.0%(最適側トl〜2%)を添加し、20
へ45℃(最適温度:30〜35℃)に保ち、約6〜4
8時間1発酵を行なわせる。ここで得られた発酵液をP
H4〜フに調整した後、二酸化炭素の発生状態を、アル
コール生成量で発酵の終了を確認した後、発酵終了液を
、デヵンテーシ醜ン、遠心分離、濾過の順序により操作
して。Add O11~5.0% (optimal side l~2%) and add 20%
Keep at 45℃ (optimal temperature: 30-35℃), about 6-4℃.
Let fermentation take place for 8 hours. The fermented liquid obtained here is P
After adjusting the temperature to H4~F, confirming the completion of fermentation by checking the state of carbon dioxide generation and the amount of alcohol produced, the fermented liquid was decanted, centrifuged, and filtered in this order.
清澄なエキスを含む溶液を得る。A clear extract-containing solution is obtained.
「実施例2」
前記1発明の構成!記載した、ベニバナ由来のrX料(
1)〜(2)の内、その1つ、又は、両方を用い、その
重量5kgに対して jJI!1水50!水含0!L良
く攪拌、R合した後、約80°Cで20分間熱処理を行
う0次に、加温を中止し、常臥で放置して冷却を待つ、
常温に至りたら、酢酸99.5%にてpH5,0附近に
溶液を調整する。“Example 2” Configuration of the above-mentioned 1 invention! The rX agent derived from safflower (
Using one or both of 1) to (2), jJI! for a weight of 5 kg. 1 water 50! Contains 0 water! After stirring well and mixing, heat treat at about 80°C for 20 minutes.Next, stop heating and leave to stand for cooling.
When the temperature reaches room temperature, adjust the solution to around pH 5.0 with 99.5% acetic acid.
次いで、酵素(例えば、上田化学工業製:セルロシンA
C)50gを添加して、約40℃で18時間程度良く攪
拌させて、酵素分解を行つた後、約80℃で20分間加
熱を行し1.酵素を失活させると共に、殺菌を行い1反
応を終了する。Next, an enzyme (for example, cellulosin A manufactured by Ueda Chemical Co., Ltd.)
C) Add 50g and stir well at about 40°C for about 18 hours to perform enzymatic decomposition, then heat at about 80°C for 20 minutes.1. The enzyme is inactivated and sterilized to complete one reaction.
ここで得られた酵素分解液を分取し、常温で放置して冷
却した後、イースト菌(ペースト状)500gとブドウ
糖2.5kgを添加し、lO%水醜化ナトリウム溶液を
用いて、pH8,0附近に調!!後、恒温槽約30℃に
て、2日間程度放匠して1発酵を行なう。The enzymatically decomposed solution obtained here was separated, left to cool at room temperature, 500 g of yeast (paste) and 2.5 kg of glucose were added, and the pH was 8.0 Nearby! ! After that, it is left to ferment for about 2 days in a thermostatic oven at about 30°C.
次に、ケイソウ±(昭和化学工業製ニラジオライト)を
用い、吸引濾過した後、さらに、得られた濾液を0.4
5pmメンブランフィルターを用いて濾過する。ここで
得られた濾液量に対して。Next, after suction filtration using diatomaceous solution ± (Niradiolite manufactured by Showa Kagaku Kogyo), the obtained filtrate was further filtered with 0.4
Filter using a 5pm membrane filter. For the amount of filtrate obtained here.
メタノール又はエタノールの濃度がl Ov/V%とな
るように、濾液に添加して、1週間以上のライタリング
放置を行い、さらに、0.2pmメンブランフィルター
を用いて再濾過を行い、約4.5見の清澄な状態のエキ
スを含む溶液を得た。Add methanol or ethanol to the filtrate so that the concentration is 1 Ov/V%, leave it for 1 week or more, and then refiltrate using a 0.2 pm membrane filter. A solution containing the extract in a clear state was obtained.
前記の実施例1〜2で示す、それぞれの抽出エキスは、
沈殿物の発生も少なく、安定な水溶性成分を含むエキス
の溶液の状態で、長期間の保存が可能である。もちろん
、特異臭は線かれており。The respective extracts shown in Examples 1 and 2 above are:
There is little precipitation, and the extract solution containing stable water-soluble components can be stored for a long period of time. Of course, the peculiar smell is delineated.
大変、芳香性のよい香りが漂うエキスの溶液状態となる
。The result is an extract solution with a very aromatic scent.
次に1本発明によるエキスについて、その理化学的特性
、又は作用(性質、効果)などについて試験すれば、第
1〜第3表に示すごとくとなり。Next, when the extract according to the present invention was tested for its physicochemical properties or actions (properties, effects), the results were as shown in Tables 1 to 3.
そのいずれもが、酵素分解して得たエキスに比べ、優れ
ていることがわかった。All of them were found to be superior to extracts obtained by enzymatic digestion.
「実験例1」
前記に記載した実施例1及び2によって得られたエキス
と、酵素を作用させて得られるエキスについて、チロシ
ナーゼ活性抑制作用について見ると、その結果は第1表
に示すごとく、実施例1及び2にようて得られたエキス
の方が、メラニン色素の生成を抑制する作用が高いこと
がわかった。"Experimental Example 1" Looking at the tyrosinase activity inhibitory effect of the extracts obtained in Examples 1 and 2 described above and the extract obtained by acting with enzymes, the results are as shown in Table 1. It was found that the extracts obtained in Examples 1 and 2 had a higher effect of suppressing the production of melanin pigment.
すなわち、ベニバナ(コウカ)中には、美白作用がある
とされているが、残渣物中にも、その効果があることが
わかった。とくに1種子の残渣物中にも、このよちな作
用があることは、これまで知られておらず、新しい発見
である。That is, while safflower (Koka) is said to have a skin-whitening effect, it was also found that the residue also has this effect. In particular, it was not previously known that the residue of a single seed had this effect, and this is a new discovery.
尚、試験に当9ては、実施例1又は2で得られたエキス
を含む溶液を、凍結乾燥した粉末をもとに、水を用いて
10倍希釈した液(表1中、これをA液と表示)を用い
て行った。In addition, in the test, a solution containing the extract obtained in Example 1 or 2 was diluted 10 times with water based on the freeze-dried powder (in Table 1, this was (indicated as liquid).
又、対比に使用した酵素分解エキスは、実施例2の工程
中で酵素反応終了後の分解液をもとに。The enzymatically decomposed extract used for comparison was based on the decomposed solution after the enzymatic reaction was completed during the process of Example 2.
酵母処理の工程のみをカットし、その後の精製化、の処
理は、実施例2に示すと同様の処理を行フて、得られた
ものを凍結乾燥して、粉末としたものをもとに、木を用
いて10倍希釈した液(表1中、これをB液と表示)を
使用した。又、実験例2〜3についでも同様に、10倍
希釈により行った。Only the yeast treatment process was cut, and the subsequent purification process was performed in the same manner as shown in Example 2, and the resultant product was freeze-dried and powdered. A solution diluted 10 times with wood (this is indicated as solution B in Table 1) was used. Further, Experimental Examples 2 and 3 were similarly carried out by 10-fold dilution.
試験法は、チロシンにチロシナーゼを作用させ、生成さ
れるメラニン色素を640nmで1反応系組成は1次に
示すごとくである。The test method is to react tyrosine with tyrosinase and measure the melanin pigment produced at 640 nm.The composition of the reaction system is as shown below.
(反応組成)
L−チロシン(1,0mg/mu)0.5mlリン酸緩
衝液(PH6,8) 2.0ffi見蒸留水又は
検体 2.OmJL銅イオン(1%溶
液) 0.05m!チロシナーゼ(1,0m
g/mJL)1.0m皇第1表 チロシナーゼ活性抑制
作用
「実験例2」
熱安定性について、ここでは、実施例2によつて得られ
たエキスと、その工程中で酵素を作用させて得られた酵
母処理をしないて得られたエキスについて、先の試験で
用いたA液とB液をもとに、試験したが、その結果は第
2表に示すととくてあり、色調は、50℃で7日間放置
した場合を除けば、酵素分解後、さらに、酵母処理を加
えて得られたエキスでは、安定であり、常温で保存が可
能であることがわかった。(Reaction composition) L-tyrosine (1.0 mg/mu) 0.5 ml phosphate buffer (PH6,8) 2.0ffi distilled water or specimen 2. OmJL copper ion (1% solution) 0.05m! Tyrosinase (1,0m
g/mJL) 1.0m Table 1 Tyrosinase activity inhibitory effect "Experimental Example 2" Regarding the thermostability, here we will discuss the heat stability of the extract obtained in Example 2 and the extract obtained by reacting with an enzyme during the process. The extract obtained without yeast treatment was tested based on the A and B solutions used in the previous test.The results are shown in Table 2, and the color tone was 50. It was found that the extract obtained by further yeast treatment after enzymatic decomposition is stable and can be stored at room temperature, except when left at 7 days at ℃.
しかし、1111g処理のみによって得られたエキスで
は、濁り、あるいは沈殿物の発生が認められ、その優劣
の差は大きく1本法による拍出法は優れていることがわ
かった。However, in the extract obtained only by the 1111g treatment, turbidity or precipitation was observed, and the difference in quality was large, and it was found that the one-tube extraction method was superior.
又、外観的にも、酵母処理した後のエキスでは、濁りの
発生は認められず、さらに、芳香性も良好であることが
わかった。Furthermore, in terms of appearance, no turbidity was observed in the extract after the yeast treatment, and furthermore, it was found to have good aromatic properties.
色調については、4フOnmで、吸光度計により測定す
る方法を採用した。The color tone was measured using an absorbance meter at 4 nm.
「実験例3」
本発明によるエキスについては、pHの影響についてみ
ると、第3表に示すごとくであった。"Experimental Example 3" Regarding the extract according to the present invention, the influence of pH was as shown in Table 3.
すなわち、pHが9.0以上では、少々の濁り、又は澱
の発生を認め、又色調もPHが9.0以上から増加傾向
を示すことがわかった。That is, it was found that when the pH was 9.0 or higher, slight turbidity or sludge was observed, and the color tone also showed an increasing tendency from the pH 9.0 or higher.
とくに、色調については、酵素分解して得られたエキス
と1本発明による酵素分解後に酵母処理したエキスも、
同じ傾向が示される。しかし、濁り又は澱の発生は、酵
母処理されたエキスは、[I然少なく、より優れている
ことがわかった。In particular, regarding the color tone, the extract obtained by enzymatic decomposition and the extract treated with yeast after enzymatic decomposition according to the present invention,
The same trend is shown. However, the occurrence of turbidity or sludge was found to be much lower and better in the yeast-treated extract.
色調については、470nmで、吸光度計により測定す
る方法を採用した。The color tone was measured using an absorbance meter at 470 nm.
尚、6表(第1〜3表)では、A液とB液、つまり、酵
母処理後のエキスと酵素分解後のエキスをもって対比し
たが、古来から知られている1mやアルカリによる分解
抽出エキスや水を用いた温湯抽出エキスを得て、これと
対比しても、水沫のよる酵母処理後のエキスの方が、安
定性に優れていることがわかつた。In addition, in Table 6 (Tables 1 to 3), liquid A and liquid B, that is, the extract after yeast treatment and the extract after enzymatic decomposition, are compared, but 1m and alkali-decomposed extracts, which have been known since ancient times, are compared. Even when compared with a hot water extract obtained using water and water, it was found that the extract after yeast treatment using water droplets was superior in stability.
m2表 −20〜80℃温度に対する影響013表 P
Hの対する影響
次表(第4表)は、ベニバナ抽出エキス、及びベニバナ
紡出エキス含有化粧水(処方例1)について見たフィー
リングテストの結果を示すものである。その結果は1本
法(実施例)に示す方法で得られたベニバナ抽出エキス
、及びベニバナ抽出エキス含有化粧水の方が、芳香性も
良好であり。m2 table -20~80℃ temperature influence 013 table P
Effect of H The following table (Table 4) shows the results of the feeling test for the lotion containing safflower extract and safflower spun extract (formulation example 1). The results showed that the safflower extract obtained by the method shown in Method 1 (Example) and the lotion containing the safflower extract had better fragrance.
肌に対するしっとり感、又は爽快感が良好に現われると
いう解答が多かった。There were many answers that the skin felt moisturized or had a refreshing feeling.
第4表 ベニバナ抽出エキスの 使用感触テスト結果 以上1本発明の実施例、実験例で示すごとく。Table 4: Safflower extract Usage feel test results As shown above in the Examples and Experimental Examples of the present invention.
ベニバナ中から美白性効果、保湿性効果の優れた糖類及
びアミノ酸を含有するエキスが得られ、化粧品への配合
性に優れている。An extract containing saccharides and amino acids with excellent whitening and moisturizing effects can be obtained from safflower, and has excellent incorporation into cosmetics.
以下に、その処方例を記す。An example of its prescription is given below.
尚、第4表及び処方中で示されるAエキスとは1本発明
の実施例1及び実施例2で得られたエキスを示し、糖類
及びアミノ酸を主体とするエキスのことをいう。Note that extract A shown in Table 4 and in the prescription refers to the extract obtained in Example 1 and Example 2 of the present invention, and refers to an extract mainly composed of saccharides and amino acids.
(処方例−1:化粧水)
Aエキス 3.0%グリセ
リン 5.01.3−ブチレン
ゲリコール 4.0オレイルアルコール
0.1ポリオキシソルビタンモノラウリ
ン酸
エステル(20E、D、) 1.5ポリオキ
シエチレンラウリル
エーテル(20E、D、) 0.5エチルア
ルコール 10.0でシネ鴫0.1
色素 適 量紫外線吸収
剤又は防腐剤 適 量精製水をもうて、全
量100となす。(Formulation Example-1: Lotion) Extract A 3.0% Glycerin 5.0 1.3-Butylene Gelicol 4.0 Oleyl Alcohol
0.1 Polyoxysorbitan monolaurate (20E, D,) 1.5 Polyoxyethylene lauryl ether (20E, D,) 0.5 Ethyl alcohol 10.0 and 0.1 Pigment Appropriate amount Ultraviolet absorber or Preservative: Add an appropriate amount of purified water to make a total volume of 100 ml.
(処方例−2:クリーム)
Aエキス S、O%ステ
アリンfi 14.0ポリオキ
シエチレンソルビタン
モノステアリン酸エステル
(20E、D、) 1.5
ワセリン 2.0モノステ
アリン霞グリセリン 2.5!、3−ブチレン
グリコール 8.0香N
O15酸化防止剤又は防腐剤
適 量精製水をもうて、全1tooとなす。(Prescription example-2: cream) A extract S, O% stearin fi 14.0 Polyoxyethylene sorbitan monostearate (20E, D,) 1.5 Vaseline 2.0 Monostearin haze glycerin 2.5! , 3-butylene glycol 8.0 N
O15 antioxidant or preservative
Add an appropriate amount of purified water to make 1 too.
(処方例−3:乳液)
Aエキス 1.0%スク
ワラン S、Oワセリン
2・Oミツロウ
0・5ソルビタセスキオレイン酸エス
テル 0.8ポリオキシエチレン
オレイルエーテル(20E、D、) 1.21.3−
ブチレンゲリコール 5.0エチルアルコール
5.0カルボキシビニールポリマ
ー
(1,0%水溶性) 20.0香料
適 量酸化防止剤又は防腐剤
適 量水酸化カリウム
0.1精製水をもって、全1tooとなす。(Formulation example-3: Emulsion) A extract 1.0% squalane S, O petrolatum
2.O beeswax
0.5 Sorbitasesquioleic acid ester 0.8 Polyoxyethylene oleyl ether (20E, D,) 1.21.3-
Butylene gellicol 5.0 Ethyl alcohol 5.0 Carboxy vinyl polymer (1.0% water soluble) 20.0 Fragrance
Appropriate amount of antioxidant or preservative Appropriate amount of potassium hydroxide
Add 0.1 purified water to make 1 too.
第5表 日局収佐の生薬
(ハ)発明の効果
従来から、ベニバナの花からは色素を、!4子からは油
を抽出していた。しかし、その残渣物に関しては、あま
り有効的な利用方法がないままになっていた。Table 5: Effects of the invention of crude drugs (c) by the Japan Bureau of Medicine Traditionally, pigments have been extracted from safflower flowers! Oil was extracted from the four children. However, there has been no effective way to utilize the residue.
すなわち、大量に除去される残渣物には、主として、デ
ンプン質や蛋臼賀、繊維質が含まれており、これをもと
に、加水分解して得られた分解液を、さらに、酵母によ
り発酵させ、香りのよいエキスとなし、さらに、糖類や
アミノ酸を主体としたエキスを得ることに成功したので
ある。In other words, the residue that is removed in large quantities mainly contains starch, protein, and fiber, and based on this, the decomposition liquid obtained by hydrolysis is further processed with yeast. By fermenting it, they were able to create a fragrant extract, and they also succeeded in obtaining an extract that was mainly composed of sugars and amino acids.
動物l&i器や薬用植物に、酵素又酸やアルカリを作用
させてなるエキスの製造法は、古くから知られているが
、さらに、酵母を作用させることを特徴とする製造法は
1本発明者らが始めてであり。Methods for producing extracts by reacting enzymes, acids, and alkalis with animal organs and medicinal plants have been known for a long time, but the present inventor has developed a method for producing extracts characterized by the action of yeast. This is the first time.
さらに1本発明による抽出エキスは、実験例に示すごと
く、チロシナーゼ活性抑制作用があり、メラニン色素の
生成を抑制するので、美白的効果が期待される。よって
、化粧品等に有効利用できるミノ醜等が含まれており、
保湿作用を有し、肌の保護剤としても優れ、化粧品に配
合することにより、肌や髪の乾燥を防ぎ、柔軟性をも与
える効果が得られる0本発明による抽出エキスは、化粧
品には、液性の化粧水をはじめ、クリームや乳液等に用
いやすく、さらに、医薬品や4a床食品などの滋養1強
壮を目的に用いることも出来る。Furthermore, as shown in the experimental examples, the extract according to the present invention has a tyrosinase activity inhibiting effect and inhibits the production of melanin pigment, so it is expected to have a whitening effect. Therefore, it contains minerals that can be effectively used in cosmetics, etc.
The extract according to the present invention has a moisturizing effect and is excellent as a skin protectant, and when incorporated into cosmetics, it can prevent dryness of the skin and hair and provide flexibility. It is easy to use in liquid lotions, creams, emulsions, etc., and can also be used for nourishing and tonic purposes such as medicines and 4A floor foods.
一方1本発明において開示された実施例1〜2の手段を
採用すれば、ベニバナのみならず、例えば1日周に収載
される第5表に示すごとくの植物系生薬類の拍出エキス
を得るに当っても有効である。On the other hand, if the means of Examples 1 and 2 disclosed in the present invention are adopted, it is possible to obtain extracts of not only safflower but also of plant-based crude drugs as shown in Table 5 listed in the daily cycle. It is also valid even if
Claims (1)
物、又は、ベニバナの種子より、サフラワー油を抽出し
た際の残渣物を出発原料となし、公知な手段により、加
水分解して得られた分解液に対して、酵母を添加して、
発酵させて得られることを特徴とするベニバナ抽出エキ
スの製造法。[Scope of Claims] [1] The starting material is a residue obtained when pigments are extracted from tubular flowers of safflower in the flowering stage, or a residue obtained when safflower oil is extracted from safflower seeds, and a known method is used. By adding yeast to the decomposition liquid obtained by hydrolysis,
A method for producing a safflower extract characterized by being obtained by fermentation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62031968A JPS63201108A (en) | 1987-02-14 | 1987-02-14 | Production of water-soluble extract extracted from flower or seed of safflower |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62031968A JPS63201108A (en) | 1987-02-14 | 1987-02-14 | Production of water-soluble extract extracted from flower or seed of safflower |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63201108A true JPS63201108A (en) | 1988-08-19 |
Family
ID=12345752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62031968A Pending JPS63201108A (en) | 1987-02-14 | 1987-02-14 | Production of water-soluble extract extracted from flower or seed of safflower |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63201108A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02234638A (en) * | 1989-03-08 | 1990-09-17 | Ajinomoto Co Inc | Method for keeping freshness of plant |
JPH0616530A (en) * | 1992-07-03 | 1994-01-25 | Mikimoto Pharmaceut Co Ltd | Cosmetic |
JPH11349435A (en) * | 1998-06-03 | 1999-12-21 | Noevir Co Ltd | Skin agent used for external use and effective for preventing and improving pigmentary symptom caused by ultraviolet light |
KR20010084402A (en) * | 2000-02-25 | 2001-09-06 | 박인배 | Safflower Seeds Extracts Inhibiting Melanin Biosynthesis and Composition Comprising Same |
KR20020074006A (en) * | 2001-03-19 | 2002-09-28 | 함양농업협동조합 | Method for preparing healthy food containing powder of carthamus tinctorius l. |
KR20030001218A (en) * | 2002-02-16 | 2003-01-06 | 이광현 | Serotonin compounds extracted from Carthamus tinctorius and compositions containing the same |
JP2004043514A (en) * | 2003-11-14 | 2004-02-12 | Noevir Co Ltd | Endothelin-1 inhibitor |
JP2005008532A (en) * | 2003-06-17 | 2005-01-13 | Eau De Vie Japon:Kk | Humectant and skin cosmetic and food and drink for beauty culture comprising the same humectant formulated therein |
JP2009263282A (en) * | 2008-04-25 | 2009-11-12 | National Institute Of Advanced Industrial & Technology | Melanogenesis inhibitor |
JP5367139B1 (en) * | 2012-09-14 | 2013-12-11 | 株式会社伊勢半 | Safflower fermented liquor |
CN106729358A (en) * | 2015-11-24 | 2017-05-31 | 郑秀芝 | A kind of tubular Chinese medicine processs bar |
-
1987
- 1987-02-14 JP JP62031968A patent/JPS63201108A/en active Pending
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02234638A (en) * | 1989-03-08 | 1990-09-17 | Ajinomoto Co Inc | Method for keeping freshness of plant |
JPH0616530A (en) * | 1992-07-03 | 1994-01-25 | Mikimoto Pharmaceut Co Ltd | Cosmetic |
JPH11349435A (en) * | 1998-06-03 | 1999-12-21 | Noevir Co Ltd | Skin agent used for external use and effective for preventing and improving pigmentary symptom caused by ultraviolet light |
KR20010084402A (en) * | 2000-02-25 | 2001-09-06 | 박인배 | Safflower Seeds Extracts Inhibiting Melanin Biosynthesis and Composition Comprising Same |
KR20020074006A (en) * | 2001-03-19 | 2002-09-28 | 함양농업협동조합 | Method for preparing healthy food containing powder of carthamus tinctorius l. |
KR20030001218A (en) * | 2002-02-16 | 2003-01-06 | 이광현 | Serotonin compounds extracted from Carthamus tinctorius and compositions containing the same |
JP2005008532A (en) * | 2003-06-17 | 2005-01-13 | Eau De Vie Japon:Kk | Humectant and skin cosmetic and food and drink for beauty culture comprising the same humectant formulated therein |
JP2004043514A (en) * | 2003-11-14 | 2004-02-12 | Noevir Co Ltd | Endothelin-1 inhibitor |
JP2009263282A (en) * | 2008-04-25 | 2009-11-12 | National Institute Of Advanced Industrial & Technology | Melanogenesis inhibitor |
JP5367139B1 (en) * | 2012-09-14 | 2013-12-11 | 株式会社伊勢半 | Safflower fermented liquor |
CN106729358A (en) * | 2015-11-24 | 2017-05-31 | 郑秀芝 | A kind of tubular Chinese medicine processs bar |
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