JP2019043942A - Method and apparatus for producing microwave dried or aging-drying polygonum tinctorium lour. leaves and use thereof - Google Patents
Method and apparatus for producing microwave dried or aging-drying polygonum tinctorium lour. leaves and use thereof Download PDFInfo
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Landscapes
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- Coloring (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
本発明は、マイクロ波乾燥あるいは熟成乾燥藍葉の製造方法、装置およびその用途に関する。
本発明において、マイクロ波熟成乾燥藍葉の「熟成」とは、生藍葉中の酵素がマイクロ波で活性化され、酵素反応が促進され、および/または酵素活性が高まることを、「熟成乾燥藍葉」とは、生藍葉中の酵素反応が促進され、および/または酵素活性が高まることにより、インジカン分解酵素活性、イサチン含有量、およびトリプタントリン含有量からなる群のいずれか一以上が、自然乾燥葉に比べて高い乾燥藍葉を、意味する。
TECHNICAL FIELD The present invention relates to a method for producing microwave-dried or matured dried mulberry leaves, an apparatus thereof and uses thereof.
In the present invention, "ripening" of microwave ripening dried mulberry leaves means that enzymes in fresh mulberry leaves are activated by microwaves to accelerate the enzyme reaction and / or increase enzyme activity. Is that by promoting the enzyme reaction in ginger leaves and / or increasing the enzyme activity, at least one of the group consisting of indican degradation enzyme activity, isatin content, and tryptanthrin content is naturally dried leaf It means higher dry mulberry leaves, compared to.
天然色素である藍を用いた染毛剤として、2種類の乾燥藍葉のみを用いた染毛剤が開発されている(特許文献1)。生藍葉を加熱してインジカン分解酵素を失活させたインジカンを含有する乾燥藍葉粉末と、インジカン分解酵素を失活させることなく、50℃以下で低温乾燥させた藍葉粉末の二つの乾燥粉末の組み合わせからなる染毛剤である。インジカンを含有する乾燥藍葉粉末と酵素活性のある低温乾燥藍葉粉末および水を混合すると、乾燥藍葉中のインジカンが酵素分解されインドキシルとなって水に溶解する。このインドキシルが酸化されてインジゴになり、条件によってはインジルビン(赤色)などが副生成するので、赤、青、黄色が任意の組み合わせで混じった茶、藍、紫、黒色に染毛させることができる。酵素分解されたインドキシルが毛髪に結合して、洗髪後にインドキシルが酸化されたインジゴが、徐々に濃厚な色に変化し、染毛が定着される。 A hair dye using only two types of dry mulberry leaves has been developed as a hair dye using a natural pigment, an eyebrow (Patent Document 1). A combination of two dry powders of dried mulberry leaf powder containing indican which has been indican denatured enzyme inactivated by heating raw mulberry leaves and mulberry leaf powder dried at low temperature below 50 ° C. without indicane degradation enzyme inactivated Hair dye. When the dry mulberry leaf powder containing indican is mixed with low temperature dry mulberry leaf powder having enzyme activity and water, the indican in the dry mulberry leaves is enzymatically decomposed to become indoxyl and dissolved in water. The indoxyl is oxidized to form indigo, and depending on the conditions, indirubin (red) is by-produced, so that red, blue, and yellow may be dyed in any combination of tea, amber, purple, and black. it can. Enzymatically degraded indoxyl binds to the hair, and after hair washing, the indoxy oxidized with indoxyl gradually changes to a thick color, and the hair is fixed.
また、藍はタデ藍ともいわれ、古来から薬用植物として使用されていることが古文書(非特許文献1)に記載されているが、近年藍葉中に含まれる有用成分であるトリプタントリン(特許文献2)、イサチン(非特許文献2)の抗アレルギー活性、抗真菌活性、神経活性物質としての効能が注目されている。 In addition, anthers are also known as Tade persimmon, and it has been described in ancient documents (Non-Patent Document 1) that they have been used as medicinal plants since ancient times, but in recent years tryptanthrin (patent literature) which is a useful component contained in mulberry leaves 2) Attention is paid to the antiallergic activity, antifungal activity and efficacy as a neuroactive substance of isatin (Non-patent document 2).
一方、マイクロ波は、極性基を持つ分子や双極子モーメントの大きな化合物を直接加熱する。例えば、農作物の乾燥・蒸留では、マイクロ波が農産物の内部の水を直接加熱し、細胞壁を内部から破砕することで、乾燥効率や有用成分の抽出の点で優れていることや、熱影響が小さく、例えば、内部のビタミンC等の栄養成分の分解が少なく、栄養価にとんだ乾燥葉を得ることが可能である。また、植物内部が加熱されるために、成分の抽出が容易で、例えば、藍葉中に含まれる有用成分、トリプタントリンをマイクロ波照射下で溶媒抽出すると迅速に抽出できる(特許文献2)。 On the other hand, microwaves directly heat molecules having polar groups and compounds having a large dipole moment. For example, in the drying and distillation of agricultural products, microwaves directly heat the water inside the agricultural products and crush the cell walls from the inside, which is superior in terms of drying efficiency and extraction of useful components, and have a thermal effect. For example, it is possible to obtain dried leaves having a low nutritive value, for example, with less decomposition of nutritional components such as vitamin C inside. In addition, since the inside of the plant is heated, extraction of the components is easy, and for example, triptanthrin contained in mulberry leaves can be rapidly extracted by solvent extraction under microwave irradiation (Patent Document 2).
酵素の活性部位はアミノ酸などであり、マイクロ波で容易に加熱され、活性化される。例えば、イースト菌を用いたパン生地を電子レンジに入れ、100〜200Wで30秒程度加熱して、濡らしたペーパータオルで包み、10分程度放置すると発酵し、大きく膨らみ、オーブンで焼くとパンが簡単にできることが知られている(非特許文献3)。 The active site of the enzyme is an amino acid or the like, which is easily heated and activated by microwave. For example, the bread dough using yeast is put in a microwave oven, heated at 100 to 200 W for about 30 seconds, wrapped with a wet paper towel, left to stand for about 10 minutes, fermented, swollen greatly, and baked in an oven to make bread easy. Is known (Non-Patent Document 3).
また、マイクロ波照射装置として、釜の内部構造を対象物の性状、量にあわせて変更可能とし、撹拌機能を有することで多用途に用いることができるマイクロ波照射装置(特許文献3)が知られており、さらに、互いに向かい合わない複数方向からマイクロ波を照射し、回転反射盤を使用することで、マイクロ波の干渉を抑制し、高い均熱性を確保したマイクロ照射装置(特許文献4)では、被照射物の温度を測定することが可能な複数のセンサの検出値に基づき、3個の照射部から照射されるマイクロ波の出力を制御する。 Moreover, as a microwave irradiation apparatus, the internal structure of the kettle can be changed according to the property and the amount of the object, and the microwave irradiation apparatus (patent document 3) that can be used for various purposes by having a stirring function is known. Furthermore, in the micro irradiation device (patent document 4) which suppressed the interference of the microwave and was able to secure high thermal uniformity by irradiating microwaves from a plurality of directions which do not face each other and using a rotary reflecting plate. The output of the microwave irradiated from three irradiation parts is controlled based on the detection value of the several sensor which can measure the temperature of a to-be-irradiated object.
乾燥藍葉の主要な用途に染毛剤がある。染毛剤として使用するには、染色成分を含む乾燥葉と酵素を含む自然乾燥葉の2種類の藍葉が必要となる。酵素を含む乾燥葉の作成には、主として自然乾燥、場合により低温乾燥が用いられていたが、いずれにしても乾燥に時間を要し、かつ、酵素活性が弱く、染毛に時間がかかるなどの問題があった。酵素活性が維持された、あるいは高められた乾燥藍葉の乾燥時間を短縮して提供することが求められる。
そこで、本発明は、酵素活性が高い状態で酵素を含む乾燥藍葉を提供すること、該乾燥藍葉を効率よく製造する方法を開発することを目的とする。
Hair dye is a major use of dry mulberry leaves. In order to use it as a hair dye, two types of mulberry leaves are required: dry leaves containing staining components and natural dry leaves containing enzymes. Although natural drying, in some cases low-temperature drying was mainly used for the preparation of dry leaves containing enzymes, in any case it takes time to dry, and the enzyme activity is weak, so it takes time to dye hair etc. There was a problem with It is required that the enzyme activity be maintained or enhanced to shorten the drying time of dried mulberry leaves.
Then, this invention aims at providing the dry mulberry leaf containing an enzyme in the state with high enzyme activity, and developing the method of manufacturing this dry mulberry leaf efficiently.
また、本発明は、インジカン分解酵素の活性が高められた状態で維持された乾燥藍葉に着目して、その用途を開発することを目的とする。より詳細には、染毛、染色用、沈殿藍用または藍顔料に適した乾燥藍葉を提供することを目的とする。 Another object of the present invention is to focus on dried mulberry leaves maintained in a state in which the activity of indican degradation enzyme is enhanced, and to develop its use. More particularly, it is an object of the present invention to provide a dry mulberry leaf suitable for dyeing hair, for dyeing, for precipitating glaze or for a glaze pigment.
さらにまた、本発明は、インジカン分解酵素の活性が高められるだけでなく、タデ藍の主要な生理活性物質に着目して、その用途を開発することを目的とする。より詳細には、医薬品用、化粧品用、石鹸用、染色用、または機能性食品用の沈殿藍または藍顔料を提供することを目的とする。 Furthermore, the present invention aims not only to enhance the activity of indican degradation enzyme, but also to develop its use, focusing on the main physiologically active substance of Tade persimmon. More specifically, it is an object of the present invention to provide a precipitated indigo or indigo pigment for pharmaceutical, cosmetic, soap, dyeing, or functional food.
藍葉中のインジカンは、刈りとられると、脱グルコース酵素の作用で、インドキシルとなり、次いで酸化されてインジゴとなる。本発明では、この酵素反応をマイクロ波で調節しながら乾燥させるもので、
(a)生藍葉中の活性な酵素を保持したまま乾燥し、インジカンと活性な酵素を含有するマイクロ波乾燥藍葉とする、および
(b)生藍葉中の酵素を活性化し、酵素反応を促進し、および/または酵素活性を高め、トリプタントリン等の機能性成分を多量に含有するマイクロ波熟成乾燥藍葉とする、
の二つの態様で生藍葉中の酵素の活性を調節する。
When the indican in mulberry leaves is harvested, it becomes indoxyl and then oxidized to indigo by the action of the deglucose enzyme. In the present invention, this enzyme reaction is dried while being controlled by microwave,
(A) drying while retaining active enzyme in ginger leaf to obtain microwave dried mulberry leaf containing indican and active enzyme, and (b) activating enzyme in ginger leaf to promote enzymatic reaction And / or increase the enzymatic activity and make it a microwave-ripened dried mulberry leaf that contains a large amount of functional components such as triptanthrin,
Regulate the activity of enzymes in ginger leaves in two ways.
より詳細には、上記(a)において、マイクロ波照射法では、生藍葉にマイクロ波を真空圧5kPa以下、温度30℃以下の条件で照射して、酵素活性を保持し、インジカンを保持したまま乾燥することができる。インジカン分解酵素は、30〜40℃では、マイクロ波照射すると、活性化し、迅速にインジカンを分解するので、マイクロ波低温減圧乾燥する際に、あらかじめ氷水等に浸漬し、冷やしておいて5kPa以下の低温で迅速乾燥する。さらに、酵素の働きを鈍らせるために、ブドウ糖、砂糖などを共存させておいて迅速乾燥することによりインジカンの分解を低減できることを見いだし、本発明に至った。 More specifically, in the above (a), in the microwave irradiation method, ginger leaf is irradiated with a microwave under a vacuum pressure of 5 kPa or less and a temperature of 30 ° C. or less to retain the enzyme activity and retain the indican It can be dried. Since the indican degradation enzyme is activated by microwave irradiation at 30 to 40 ° C and rapidly decomposes the indican, it is immersed in ice water etc. beforehand when it is dried by microwave low-temperature low-pressure drying, and it is cooled to 5 kPa or less Dry quickly at low temperatures. Furthermore, in order to slow down the function of the enzyme, it was found that the decomposition of indican can be reduced by rapid drying in the coexistence of glucose, sugar and the like, and the present invention has been achieved.
藍葉を加熱してインジカン分解酵素を失活させたインジカンを含有する乾燥藍葉粉末と、インジカン分解酵素を失活させることなく、50℃以下で乾燥させた藍葉粉末の二つの乾燥粉末の組み合わせからなる染毛剤を製造するに際し、50℃以下の低温乾燥として自然乾燥あるいは定温乾燥機を用いると、乾燥に数日要し、また、得られた乾燥藍葉のインジカン分解酵素の活性がいずれも低く、染毛時に発色時間が長くなり、また、発色がばらつくなどの問題があった。
藍葉を低温乾燥させる前に、大気圧下、マイクロ波照射下、50℃以下、好ましくは40℃以下の条件で熟成すると、藍葉が緑色から濃緑色に変化し、インジカンが無くなり、インジゴとなっていることを認め、この熟成藍葉を低温マイクロ波減圧乾燥した結果、本乾燥藍葉にはインジカン分解酵素(β-グルコシダーゼ)の高い活性度を保持したまま乾燥藍葉が得られることを見出し、本発明を完成するに至った。
上記(b)において、生藍葉に30〜50℃、望ましくは40℃以下の低温下でマイクロ波を照射することにより、藍葉中の酵素を活性化、酵素反応を促進させ、酵素活性が高まった熟成藍葉を50℃以下の温度でマイクロ波減圧乾燥し、酵素活性が高まった状態を維持して乾燥することを特徴とする藍葉の低温マイクロ波熟成乾燥方法、およびマイクロ波熟成乾燥藍葉またはその粉末や抽出物とその用途に関する。
It consists of a combination of two dry powders of dried mulberry leaf powder containing indican which has been indican denatured enzyme inactivated by heating mulberry leaves, and mulberry leaf powder dried at 50 ° C. or less without indican degradation enzyme being inactivated. When producing a hair dye, using natural drying or a constant temperature drier as low-temperature drying at 50 ° C. or less requires several days for drying, and the activity of the indican degrading enzyme of the resulting dried persimmon leaf is low, Coloring time is prolonged at the time of hair dyeing, and there are also problems such as uneven coloring.
When mulberry leaves are ripened under conditions of 50 ° C. or less, preferably 40 ° C. or less under microwave irradiation under atmospheric pressure before low-temperature drying, mulberry leaves change from green to dark green, indican disappears, and indigo As a result of low-temperature microwave drying of the matured mulberry leaves, it was found that dried mulberry leaves can be obtained while maintaining high activity of indican degradation enzyme (β-glucosidase) in the dried mulberry leaves. It came to complete.
In the above (b), by irradiating microwaves to ginger leaves at a low temperature of 30 to 50 ° C., preferably 40 ° C. or less, the enzymes in mulberry leaves are activated and the enzyme reaction is promoted to enhance the enzyme activity A low temperature microwave ripening and drying method of mulberry leaves characterized in that ripening mulberry leaves are dried under reduced pressure at a temperature of 50 ° C. or lower under microwave reduced pressure, and enzyme activity is maintained and dried, and microwave ripening dried mulberry leaves or powder thereof And extracts and their uses.
酵素活性を高め、機能性成分を作らせる条件として、酵素とインジカンの接触機会を増やすこと、みじん切り、水の存在、マイクロ波の低出力間欠照射が高出力連続照射より望ましい。5kPa以下で迅速乾燥させる場合は、高出力のマイクロ波を短時間に照射し、水分量の低下とともに出力を下げることが望ましい。この場合、藍植物の軸があると、マイクロ波が集中し、焦げが生じることがあるため、軸を除いておいた方が安全である。なお、棚あるいはカゴの上に藍葉を置き、下部に水を下部に於いて置く方が、余剰のマイクロ波を水に吸収させ、焦がさずに乾燥できるため、安全である。
このように低温マイクロ波熟成藍葉は、インジカン分解酵素の活性が高められるだけでなく、タデ藍の主要な生理活性物質であり、抗菌活性、抗アレルギー活性を有するトリプタントリンおよび神経活性物質であるイサチンが自然乾燥葉の1.5〜66倍以上もの高濃度で含有することが確認された。
よって、本発明は、そのままの状態ではもちろんのこと、水等の溶媒で抽出した藍エキスや沈殿藍、藍顔料として、機能性食品、化粧品、染毛素材、染色素材、石鹸および医薬品としての用途にも用いられる高機能性乾燥藍葉、その粉末およびその抽出物を提供するに至った。
As conditions for enhancing the enzyme activity and producing the functional component, it is desirable to increase the contact opportunity between the enzyme and the indican, chopped, presence of water, low power intermittent irradiation of microwaves than high power continuous irradiation. In the case of rapid drying at 5 kPa or less, it is desirable to irradiate high-power microwaves in a short time, and to decrease the output as the water content decreases. In this case, it is safer to leave the axis, since microwaves may be concentrated and burnt may occur if there is an axis of a rattan plant. It is safer to place mulberry leaves on a shelf or a basket and put water at the lower part, because excess microwaves can be absorbed by the water and dried without burning.
Thus, low temperature microwave ripening mulberry leaves not only enhance the activity of indican degradation enzyme, but also are the main physiologically active substances of Tade persimmon, and trypanthrin having antibacterial activity, antiallergic activity and isatin which is a neuroactive substance. It has been confirmed that it contains at a concentration as high as 1.5 to 66 times that of naturally dried leaves.
Therefore, the present invention is used not only as it is, but also as extract of persimmon extract and precipitated persimmon extracted with a solvent such as water, and persimmon pigment, functional food, cosmetics, hair dye material, dyeing material, soap and medicine It came to provide a highly functional dry mulberry leaf which is also used, its powder and its extract.
本発明は以下の(1)ないし(7)の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法を要旨とする。
(1)生藍葉のマイクロ波乾燥あるいは熟成乾燥方法において、マイクロ波照射により生藍葉中の酵素の活性を調節して、通常の低温乾燥及びマイクロ波減圧乾燥藍葉に比べ、乾燥藍葉中の機能性物質量を高く保持あるいは増加させることを特徴とする方法。
(2)生藍葉中の酵素の活性の調節が、生藍葉中の酵素活性を制御することであり、生藍葉にマイクロ波を真空圧5kPa以下、温度30℃以下の条件で照射して、インジカン含有量を高く保持したまま活性な酵素を含有する乾燥藍葉を製造する、上記(1)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
(3)生藍葉中の酵素の活性の調節が、生藍葉中のインジカン分解酵素の働きを制御することであり、刈りとった後、氷を加えて30℃以下に冷却した藍葉を用いることにより行われる、上記(1)または(2)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
(4)生藍葉中の酵素の活性の調節が、生藍葉中のインジカン分解酵素の働きを制御することであり、刈りとった後、ブドウ糖、砂糖または酒の粕を含有する水溶液に2分〜30分浸漬した藍葉を用いることにより行われる、上記(1)または(2)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
(5)生藍葉中の酵素の活性の調節が、藍葉内の酵素を活性化するとともに酵素反応を促進することであり、生藍葉を30〜40℃に制御しながらマイクロ波を間欠的に所定時間照射し、藍葉内の酵素を活性化するとともに酵素反応を促進し、その後10kPa、40℃以下の温度でマイクロ波減圧乾燥して、機能性物質量が増加した熟成乾燥藍葉を製造する、上記(1)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
(6)前記の所定時間が5〜30分である、上記(5)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
(7)生藍葉がみじん切りした生藍葉である、上記(5)または(6)に記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法。
The present invention is summarized by the following methods (1) to (7) of the method for microwave drying or ripening drying of ginger leaves.
(1) In microwave drying or ripening drying method of ginger leaf, the activity of the enzyme in ginger leaf is adjusted by microwave irradiation, and compared with the usual low temperature drying and microwave decompression dry mulberry leaf, the functionality in dried mulberry leaf A method characterized in that the amount of substance is kept high or increased.
(2) The regulation of the activity of the enzyme in ginger leaf is to control the enzyme activity in ginger leaf, and the ginger leaf is irradiated with a microwave under a vacuum pressure of 5 kPa or less and a temperature of 30 ° C. or less, The microwave drying or the ripening drying method of the ginger leaf as described in said (1) which manufactures the dry mulberry leaf containing an active enzyme, hold | maintaining content high.
(3) The regulation of the activity of the enzyme in ginger leaves is to control the function of the indican degradation enzyme in ginger leaves, and after harvesting, by using ice leaves added and cooling to 30 ° C. or less The microwave drying or the ripening drying method of the ginger leaf as described in said (1) or (2) performed.
(4) The regulation of the activity of enzymes in ginger leaves is to control the action of indican degradation enzymes in ginger leaves, and after harvesting, it takes 2 minutes to an aqueous solution containing glucose, sugar or sake lees The microwave drying or the ripening drying method of the ginger leaf as described in said (1) or (2) performed by using the mulberry leaf which was immersed for 30 minutes.
(5) The regulation of the activity of the enzyme in ginger leaves is to activate the enzyme in the mulberry leaves and promote the enzyme reaction, and intermittently control microwaves at 30 to 40 ° C. while controlling the ginger leaves at 30 to 40 ° C. Irradiate for a time to activate the enzyme in mulberry leaves and accelerate the enzyme reaction, and then dry under reduced pressure at a temperature of 10 kPa, 40 ° C. or less under microwave pressure to produce mature dried mulberry leaves with increased functional substance mass, The microwave drying or the ripening drying method of the ginger leaf as described in (1).
(6) The microwave drying or the ripening drying method of the ginger leaf as described in said (5) whose said predetermined time is 5 to 30 minutes.
(7) A method for microwave drying or ripening drying of ginger leaf according to the above (5) or (6), wherein the ginger leaf is a freshly chopped ginger leaf.
また、本発明は以下の(8)および(9)の乾燥藍葉組成物の製造方法を要旨とする。
(8)藍葉を大気圧下、70℃以上で1〜30分間加熱し、酵素を失活させた後、減圧して室温まで冷やして酵素を失活させた藍葉を得、その藍葉に重量比で1/5〜1/10の生藍葉を加えて、上記(5)ないし(7)のいずれかに記載の方法を適用する、機能性物質量が増加した熟成乾燥藍葉および藍葉中の酵素が失活している乾燥藍葉の混合物からなる乾燥藍葉組成物の製造方法。
(9)機能性物質量が増加した熟成乾燥藍葉が、インジカン分解酵素活性、イサチン含有量、およびトリプタントリン含有量からなる群のいずれか一以上が、自然乾燥葉に比べて高いものである、上記(8)に記載した乾燥藍葉組成物の製造方法。
The present invention also provides a method of producing the dried mulberry leaf composition of the following (8) and (9).
(8) The persimmon leaf is heated at 70 ° C. or higher for 1 to 30 minutes under atmospheric pressure to inactivate the enzyme and then decompressed and cooled to room temperature to obtain persimmon leaf with the enzyme inactivated, the weight ratio of persimmon leaf is Add 1/5 to 1/10 ginger leaves and apply the method according to any of the above (5) to (7), and the enzyme in mature dried mulberry leaves and mulberry leaves with increased functional substance mass is Process for producing a dry mulberry leaf composition comprising a mixture of inactivated dry mulberry leaves.
(9) A matured dry mulberry leaf with increased functional substance mass is higher in any one or more of the group consisting of indican degradation enzyme activity, isatin content, and triptanthrin content compared to natural dry leaf, The manufacturing method of the dried mulberry leaf composition described in said (8).
また、本発明は以下の(10)の食品素材用、化粧品素材、または医薬品素材として用いる方法を要旨とする。
(10)上記(1)ないし(7)のいずれかに記載の方法で得られたマイクロ波乾燥あるいは熟成乾燥葉そのもの、または上記(8)または(9)の方法で得られた乾燥藍葉組成物そのもの、または該マイクロ波乾燥あるいは該熟成乾燥葉または該乾燥藍葉組成物を水、溶媒で抽出したエキスを食品素材用、化粧品素材、または医薬品素材として用いる方法。
In addition, the present invention is summarized as a method of using as a food material, a cosmetic material, or a pharmaceutical material of the following (10).
(10) The microwave-dried or ripened dry leaf itself obtained by the method according to any one of the above (1) to (7), or the dried mulberry leaf composition obtained by the method according to the above (8) or (9) A method of using the extract obtained by itself, or the microwave dried or the matured dried leaf or the dried persimmon leaf composition extracted with water or a solvent as a food material, a cosmetic material or a pharmaceutical material.
また、本発明は以下の(11)の染毛方法を要旨とする。
(11)上記(1)ないし(7)のいずれかに記載の方法で得られたマイクロ波乾燥あるいは熟成乾燥葉、または上記(8)または(9)に記載の方法で得られた乾燥藍葉組成物に、2〜20倍の水を加えてペースト状にし、髪に塗布した後洗髪すること特徴とする染毛方法。
Moreover, this invention makes it the summary the hair-dyeing method of the following (11).
(11) Microwave-dried or ripened dry leaf obtained by the method according to any of the above (1) to (7), or dry mulberry leaf composition obtained by the method according to the above (8) or (9) 2 to 20 times the amount of water is added to the product to form a paste, which is applied to the hair and then the hair is washed.
また、本発明は以下の(12)の染色方法を要旨とする。
(12)上記(1)ないし(7)のいずれかに記載の方法で得られたマイクロ波乾燥あるいは熟成乾燥葉、または上記(8)または(9)に記載の方法で得られた乾燥藍葉組成物に、5〜50倍の水を加え、良くもみ、色素を水に抽出した後、藍葉をろ別した溶液中に、布を入れ、染色することを特徴とする染色方法。
Moreover, this invention makes it the summary the dyeing | staining method of the following (12).
(12) Microwave-dried or ripened dry leaf obtained by the method according to any one of the above (1) to (7) or dry mulberry leaf composition obtained by the method according to the above (8) or (9) Water is added 5 to 50 times to the material, and the dye is extracted into water, and then a cloth is placed in a solution obtained by filtering off mulberry leaves, followed by dyeing.
また、本発明は以下の(13)の医薬品用、化粧品用、石鹸用、染色用、または機能性食品用沈殿藍の調製方法を要旨とする。
(13)上記(1)ないし(7)のいずれかに記載の方法で得られたマイクロ波乾燥あるいは熟成乾燥葉、または上記(8)または(9)に記載の方法で得られた乾燥藍葉組成物を水に懸濁した水溶液に、石灰を加え、空気酸化させることを特徴とする、医薬品用、化粧品用、石鹸用、染色用、または機能性食品用沈殿藍の調製方法。
The present invention also provides a method of preparing a precipitate for use in medicine, cosmetics, soap, dyeing, or functional food according to the following (13).
(13) Microwave-dried or ripened dry leaf obtained by the method according to any of the above (1) to (7), or dry mulberry leaf composition obtained by the method according to the above (8) or (9) Lime is added to an aqueous solution in which a substance is suspended in water, and air oxidation is performed. A method for preparing a precipitate for medical use, cosmetic, soap, dyeing, or functional food.
また、本発明は以下の(14)または(15)の医薬品用、化粧品用、石鹸用、染色用、または機能性食品用藍顔料の調製方法を要旨とする。
(14)上記(1)ないし(7)のいずれかに記載の方法で得られたマイクロ波乾燥あるいは熟成乾燥葉、または上記(8)または(9)に記載の方法で得られた乾燥藍葉組成物を水に懸濁した水溶液に、タンパク質及び/または糖を加え、空気酸化させることを特徴とする、医薬品用、化粧品用、石鹸用、染色用、または機能性食品用藍顔料の調製方法。
(15)さらに、上記医薬品用、化粧品用、石鹸用、染色用、または機能性食品用藍顔料を、腸溶性物質でコーティングする工程を含む、上記(14)に記載の医薬品用、化粧品用、石鹸用、染色用、または機能性食品用藍顔料の調製方法。
In addition, the present invention is summarized as the following method (14) or (15) for a method for preparing a cosmetic, cosmetic, soap, dyeing, or functional food-grade amber pigment according to (14) or (15).
(14) Microwave-dried or ripened dry leaf obtained by the method according to any of the above (1) to (7), or dry mulberry leaf composition obtained by the method according to the above (8) or (9) A method of preparing an eyebrow pigment for pharmaceuticals, cosmetics, soaps, dyes, or functional foods, which comprises adding proteins and / or sugars to an aqueous solution obtained by suspending a substance in water and oxidizing the air.
(15) The pharmaceutical or cosmetic product according to the above (14), which further comprises the step of coating the pharmaceutical, cosmetic, soap, dyeing, or functional food-grade chewing pigment with an enteric substance. A process for the preparation of an eyebrow pigment for soap, dyeing or functional food.
また、本発明は以下の(16)及び(17)のマイクロ波照射装置を要旨とする。
(16)被照射物が収納される加熱釜と、
加熱釜に接続される導波管と、
被照射物の温度を測定する温度センサと、
マイクロ波発振器と、
温度センサからの信号に基づきマイクロ波発振器を制御する制御プログラムを格納した記憶装置を備える制御装置とを備え、
前記制御プログラムが、上記(1)ないし(7)のいずれかに記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法を実行するための制御を行うことを特徴とするマイクロ波照射装置。
釜内部に撹拌機あるいは回転の棚を着脱可能とし、藍葉を直接釜に入れ、マイクロ波減圧乾燥し、水分含量が50%以下になると棚あるいはカゴに入れ替えて、下部に水を入れ、マイクロ波減圧乾燥することが望ましい。
(17)さらに、外部からの冷却機構を付属させた上記(16)に記載のマイクロ波照射装置。
Moreover, this invention makes it a summary the microwave irradiation apparatus of the following (16) and (17).
(16) A heating pot in which the object to be irradiated is stored,
A waveguide connected to the heating kettle,
A temperature sensor that measures the temperature of the object to be irradiated;
Microwave oscillator,
A controller comprising a storage device storing a control program for controlling the microwave oscillator based on a signal from the temperature sensor;
A microwave irradiation apparatus characterized in that the control program performs control for executing the microwave drying or the ripening drying method of ginger leaf according to any one of the above (1) to (7).
Agitators or a rotating shelf can be attached and removed inside the kettle, mulberry leaves are put directly into the kettle, microwave vacuum drying is carried out, the water content becomes 50% or less, it is replaced with a shelf or basket, water is put in the lower part, microwave It is desirable to dry under reduced pressure.
(17) The microwave irradiation apparatus according to (16), further including an external cooling mechanism.
藍はタデ藍ともいわれ、タデ科イヌタデ属の一年生植物であり、水耕または露地栽培される。藍葉にはグルコースの付いたインジカンが含まれており、葉に水が供給されなくなると、インジカン分解酵素が働き、インドキシルとして溶解してくる。このインドキシルが酸化されインジゴになる。条件によってはインジルビン(赤色)などが副生成する。インドキシルは、空気にさらすなど穏やかに酸化すると、インドキシルの2分子が酸化的に結合してインジゴ(青色)に変換される。一方、インジルビンはインジゴの異性体であり、インドキシルが単分子的に酸化されてイサチンができると、未酸化のインドキシルと結合してインジルビンができる。一般に、インドキシルからインジルビンを多く生成させる条件は、pH10〜12のアルカリ性条件や高温が好ましい。紫色は、このインジゴとインジルビンが混ざった色であり、単一の紫色素ではない。赤味か青味の紫になるかは、インドキシルから、ニ方向の酸化のどちらが起こりやすいかによって決まる。 The persimmon, which is also called Tade persimmon, is an annual plant of the genus Inode, which is hydroponic or field grown. Persimmon leaves contain indican with glucose, and when water is not supplied to the leaves, indican degradation enzymes work and dissolve as indoxyl. This indoxyl is oxidized to be indigo. Depending on the conditions, indirubin (red) etc. are by-produced. When indoxyl is gently oxidized by exposure to air, two molecules of indoxyl are oxidatively bound and converted to indigo (blue). On the other hand, indirubin is an isomer of indigo, and when indoxyl is monomolecularly oxidized to form isatin, it combines with unoxidized indoxyl to form indirubin. In general, alkaline conditions at a pH of 10 to 12 and high temperatures are preferable as the conditions for generating a large amount of indirubin from indoxyl. Purple is a mixture of this indigo and indirubin, not a single purple pigment. Whether it becomes reddish or bluish purple depends on whether indoxyl or bi-directional oxidation is more likely to occur.
特許文献1に記載の2種類の乾燥藍葉とは、素早く酵素を失活させてインジカンを閉じ込めた乾燥藍葉粉末に、酵素活性を有する乾燥藍葉粉末中の酵素を作用させて染毛するものである。藍葉中に存在する酵素のうち、インジカンを分解してインドキシルを生成するインジカン分解酵素の活性が染毛のために重要である。酵素活性を有する藍葉の50℃以下での乾燥法として、室温で乾燥する自然乾燥法や定温乾燥機による低温乾燥法を用いているが、時間がかかるうえ、酵素活性を測定した結果、低温乾燥法で得られた乾燥藍葉のインジカン分解酵素の活性が低かった。 The two types of dry mulberry leaves described in Patent Document 1 are those that cause enzymes in the dry mulberry leaf powder having an enzyme activity to act on the dry mulberry leaf powder in which the indican is trapped by quickly inactivating the enzyme. . Among the enzymes present in mulberry leaves, the activity of an indican degrading enzyme that degrades indican to form indoxyl is important for dyeing. The natural drying method of drying at room temperature or the low temperature drying method with a constant temperature dryer is used as the drying method of mulberry leaves having enzyme activity at 50 ° C. or less, but it takes time and the enzyme activity is measured. The activity of the indican degradation enzyme of dried mulberry leaves obtained by the method was low.
本発明では、マイクロ波を照射しながら、インジカン分解酵素の働きを制御しながら、低温で迅速乾燥して、インジカンと活性な酵素を含有する乾燥藍葉を一段で迅速乾燥して製造する。
刈りとった藍葉を低温に保持した後、マイクロ波減圧蒸留装置に投入し、5kPa以下の高真空下で迅速乾燥する。なお、酵素の働きを制御するために、1〜5%ブドウ糖、砂糖、酒の粕、次亜塩素酸水溶液に数分浸漬した後、5kPa以下、30℃以下の温度で迅速乾燥することにより、インジカンの分解を押さえ、インジカンと活性な酵素を含有する乾燥藍葉を調整する。
In the present invention, while the action of the indican degrading enzyme is controlled while being irradiated with microwaves, rapid drying is carried out at a low temperature to rapidly dry in one step the dried mulberry leaves containing the indican and the active enzyme.
The cut mulberry leaves are kept at a low temperature, then placed in a microwave vacuum distillation apparatus, and rapidly dried under a high vacuum of 5 kPa or less. In addition, in order to control the function of the enzyme, after being immersed in 1 to 5% glucose, sugar, rice bran, hypochlorous acid aqueous solution for several minutes, and rapidly drying at a temperature of 5 kPa or less and 30 ° C. or less Control the decomposition of indican and prepare dried mulberry leaves containing indican and active enzymes.
さらに、生藍葉とマイクロ波加熱ブランチング葉を1:5〜1:10の割合で混ぜて5kPa、30℃以下で迅速乾燥し、インジカン濃度の高い、活性酵素を含有した乾燥藍葉を製造できる。 Further, ginger leaf and microwave-heated blanched leaf are mixed at a ratio of 1: 5 to 1:10 and rapidly dried at 5 kPa and 30 ° C. or less to produce a dried mulberry leaf containing a high indican concentration and containing an active enzyme.
本発明の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法は、生藍葉に温度を30〜50℃、望ましくは40℃以下に制御しながらマイクロ波照射して、酵素を活性化するとともに、酵素反応を促進、熟成して藍葉を熟成させた後、50℃以下の温度で乾燥する方法である。活性化される酵素には、インジカン分解酵素だけでなく、藍葉中に含まれる有用成分であるトリプタントリンやイサチンを合成する酵素が含まれる。藍葉あるいは沈殿藍からトリプタントリンを抽出することは特許文献2に示されているが、本発明のマイクロ波熟成乾燥藍葉はそのような抽出法の原料として最適である。 The microwave drying or ripening drying method of ginger leaves according to the present invention is performed by irradiating the ginger leaves with microwave while controlling the temperature to 30 to 50 ° C., preferably 40 ° C. or less to activate the enzyme and to activate the enzyme reaction. It is a method of promoting and ripening mulberry leaves and then drying at a temperature of 50 ° C. or less. Enzymes to be activated include not only indican degradation enzymes, but also enzymes that synthesize tryptanthrin and isatin, which are useful components contained in mulberry leaves. Although extracting triptanthrin from mulberry leaves or precipitated mulberry leaves is disclosed in Patent Document 2, the microwave ripening dry mulberry leaves of the present invention are most suitable as raw materials for such extraction methods.
低温マイクロ波熟成乾燥は、まず、生藍葉の温度を30〜50℃に温度制御しながら、1〜60分間マイクロ波照射して、生藍葉中のインジカン分解酵素を活性化させて、酵素反応を促進して藍葉を熟成させる。藍葉中の酵素は30〜40℃で活発化し、50℃を超えると活性が落ちるので、40℃以下の温度がよく、好ましくは35℃〜40℃に温度制御する。
またマイクロ波照射は連続照射より、間欠的に照射しながら熟成することが望ましい。生藍葉の温度は、光ファイバー温度計で測定し、特許文献4に記載の被照射物の温度を測定することが可能な複数のセンサを有するマイクロ波照射装置を用い、空気を移動させて測定する。
The low-temperature microwave ripening drying is performed by microwave irradiation for 1 to 60 minutes while controlling the temperature of ginger leaf to 30 to 50 ° C. to activate the indican degrading enzyme in ginger leaf to activate the enzyme reaction Promote to mature mulberry leaves. Since the enzyme in mulberry leaves becomes active at 30 to 40 ° C., and the activity drops when it exceeds 50 ° C., the temperature is preferably 40 ° C. or less, preferably 35 ° C. to 40 ° C.
In addition, it is desirable that the microwave irradiation be aged while being intermittently irradiated, rather than continuous irradiation. The temperature of ginger leaf is measured with a fiber optic thermometer, and it is measured by moving air using a microwave irradiator having a plurality of sensors capable of measuring the temperature of the irradiated object described in Patent Document 4. .
マイクロ波照射熟成の間、藍葉の重量はほとんど変化しない。マイクロ波照射は、大気圧下か、微減圧下でマイクロ波照射する。微減圧下では気流が確保されて均一に加熱されるというメリットがある。なお、低温でマイクロ波加熱する場合、マイクロ波出力および加熱時間(デューティ比を下げ)を低く抑え、低温・均一加熱下で熟成処理する。また、熟成処理は減圧下ではなく、酸素が多く存在する大気圧近辺で処理する。生成したインドキシルの酸化によるインジゴの生成は酸素が必要である。逆に、真空中もしくは不活性ガス雰囲気下で熟成処理をすることで、インジルビンを多く含む熟成乾燥藍葉も作成可能である。 During microwave irradiation aging, the weight of mulberry leaves hardly changes. The microwave irradiation is performed under atmospheric pressure or slightly under reduced pressure. Under slight pressure reduction, there is an advantage that the air flow is secured and the heating is uniform. When microwave heating is performed at a low temperature, the aging process is performed under low temperature and uniform heating while suppressing the microwave output and the heating time (reducing the duty ratio) to a low level. In addition, the aging treatment is not performed under reduced pressure, but is performed near atmospheric pressure where a large amount of oxygen is present. The formation of indigo by oxidation of the formed indoxyl requires oxygen. Conversely, ripening dried in leaf or in an inert gas atmosphere can also produce ripened dry mulberry leaves rich in indirubin.
さらに、マイクロ波照射の前に、生藍葉をみじん切りにして葉の面積を増やすことにより、酵素と基質(インジカン)の接触効率が高まり、酵素反応が活発化するので好ましい。生藍葉をみじん切りにした場合には、生藍葉重量の約10%程度の水を加えて、酵素とインジカンとの接触をさらに効率的に行わせながら、マイクロ波照射するとよい。 Furthermore, it is preferable that the contact efficiency between the enzyme and the substrate (indican) is increased by mincing ginger leaves and increasing the area of the leaves before microwave irradiation, and the enzyme reaction is activated. When ginger leaf is minced, it is preferable to add water of about 10% of ginger leaf weight to perform microwave irradiation while more efficiently contacting the enzyme with the indican.
マイクロ波照射による熟成後、活性化酵素を含有する藍葉を50℃以下の温度で、マイクロ波減圧乾燥法で素早く乾燥させ、酵素活性を維持した状態にする。酵素は水が少なくなると活動を停止し、活性なまま閉じ込められるので、マイクロ波減圧乾燥法で素早く乾燥させることが望ましい。葉の重量が60%程度まで減少するまでマイクロ波減圧乾燥を行う。なお、マイクロ波熟成後、40℃以下の定温乾燥あるいは自然乾燥でもよいが、若干酵素活性が低下する。 After ripening by microwave irradiation, mulberry leaves containing the activated enzyme are quickly dried by microwave vacuum drying at a temperature of 50 ° C. or less to maintain enzyme activity. It is desirable that the enzyme be rapidly dried by microwave vacuum drying, as the enzyme ceases activity when it is low in water and is trapped active. Microwave vacuum drying is performed until the weight of the leaves is reduced to about 60%. After microwave aging, constant temperature drying at 40 ° C. or lower or natural drying may be used, but the enzyme activity is slightly reduced.
マイクロ波熟成、減圧乾燥後、さらに乾燥藍葉の重量減少がなくなるまで完全に乾燥して、水分をなくして酵素の活動を停止させて粉末化する。乾燥方法は、たとえば、自然乾燥、40℃でのマイクロ波減圧乾燥、40℃での定温乾燥が適用できる。 After microwave ripening and drying under reduced pressure, the dried mulberry leaves are completely dried until the weight loss of the dried mulberry leaves disappear, the water is removed, and the activity of the enzyme is stopped and powdered. As a drying method, for example, natural drying, microwave vacuum drying at 40 ° C., isothermal drying at 40 ° C. can be applied.
製造したマイクロ波乾燥あるいは熟成乾燥の藍葉を染毛に用いる場合には、インジカンと酵素を同時に保持した乾燥葉粉末を作り、それを用い2〜10倍の水を加えてペースト状にして、良くもんで、インドキシルを生成させた後、髪に塗布して5〜15分以上経過後、洗髪する。染色に用いる場合には、5〜6倍の水を加えて良くもんで色素を水に抽出させてから、藍葉をろ別して染色溶液とし、布を入れて染色する。必要に応じ、インジカンと酵素を同時に保持した乾燥葉粉末を熟成乾燥藍葉粉末、あるいはそれらのいずれかと酵素を失活させてインジカンを閉じ込めた乾燥藍葉粉末の2種類の乾燥藍葉粉末に代えて用いることもできる。 When using mulberry leaves produced by microwave drying or ripening drying for dyeing hair, make a dry leaf powder that simultaneously holds indican and enzymes, and use it to make a paste by adding 2 to 10 times water. After the indoxyl is generated, it is applied to the hair, and after 5 to 15 minutes, it is shampooed. When used for dyeing, 5 to 6 times water is added and the dye is well extracted by extraction with water, and then the mulberry leaves are separated by filtration to obtain a dyeing solution, and a cloth is added for dyeing. If necessary, replace the dry leaf powder that simultaneously holds indican and enzyme with two types of dry mulberry leaf powder: ripened dry mulberry leaf powder, or dry mulberry leaf powder that inactivates the enzyme with any of them and indican is trapped. You can also.
沈殿藍用とする場合には、インジゴと酵素を含有する乾燥藍葉を水に懸濁し、インドキシルが溶出した水溶液に、あるいは、機能性物質量が増加した熟成乾燥藍葉粉末と酵素を失活させてインジカンを閉じ込めた乾燥藍葉粉末の2種類の乾燥藍葉粉末を水に懸濁した水溶液に、石灰を加えてアルカリ性して、空気酸化によりインジゴを生成させ、そのまま静置してインジゴを沈殿させて上澄み液を除去して、藍色の沈殿藍を調製する。そのまま、あるいは乾燥して藍染め染色に用いるだけでなく、青色の着色料として、かつ、抗菌活性、抗アレルギー活性を有するトリプタントリンおよび神経活性物質であるイサチンが多く含まれているので、そのまま食する青色の機能性食品として、または石鹸、化粧品および抗菌、抗アレルギー、神経活性物質としての医薬品とすることが可能である。低酸素もしくは不活性ガス雰囲気下で同様の処理をすると、インジルビンを多く含む沈殿藍の調製も可能である。
さらに、マイクロ波熟成乾燥藍葉または抽出物には青色でないが、抗菌活性、抗アレルギー活性を有するトリプタントリンや神経活性物質であるイサチンが高濃度で含有されているので、高機能性乾燥藍葉またはその抽出物は、機能性食品素材、化粧品素材および抗菌、抗アレルギー、またはパーキンソン病等に効果のある神経活性物質としての医薬品素材として使用できる。
When it is used for precipitation, the dried mulberry leaf containing indigo and the enzyme is suspended in water, and the indoxyl is dissolved in an aqueous solution in which the indoxyl is eluted, or the matured dried mulberry leaf powder and enzyme inactivated in functional substance are inactivated. Lime is added to an aqueous solution obtained by suspending two types of dry mulberry powder containing dried indica powder in water and suspended in water to form an indigo by air oxidation, leaving it as it is to precipitate indigo The supernatant is removed to prepare an amber precipitate. Not only is it used as it is or dried and dyed for dyeing, but it contains a large amount of triptanthrin having an antibacterial activity and an antiallergic activity, and a neuroactive substance isatin as a blue coloring material, so it is possible to eat as it is. It is possible to use as a blue functional food or as a medicine as a soap, cosmetics and antibacterial, antiallergic, neuroactive substance. The same treatment in a low oxygen or inert gas atmosphere also enables preparation of a precipitate containing a large amount of indirubin.
Furthermore, the microwave-ripened dried mulberry leaf or extract is not blue but contains a high concentration of triptanthrin having an antibacterial activity and an antiallergic activity and the neuroactive substance isatin, so that the highly functional dried mulberry leaf or its The extract can be used as a functional food material, a cosmetic material and a pharmaceutical material as a neuroactive substance effective for antibacterial, antiallergic or Parkinson's disease and the like.
本発明の機能性食品は、特定の疾病などを予防する健康食品、予防医薬品の分野の利用に適している。特定の疾病を予防する健康食品においては、必須成分である乾燥藍葉またはその抽出物の他に、任意的成分として、通常食品に添加されるビタミン類、炭水化物、色素、香料など適宜配合することができる。食品は液状または固形の任意の形態で食することができる。ゼラチンなどで外包してカプセル化した軟カプセル剤として食することができる。カプセルは、例えば、原料ゼラチンに水を加えて溶解し、これに可塑剤(グリセリン、D−ソルビトールなど)を加えることにより調製したゼラチン皮膜でつくられる。 The functional food of the present invention is suitable for use in the fields of health food and preventive medicine that prevent specific diseases and the like. In health foods that prevent specific diseases, vitamins, carbohydrates, pigments, flavors, etc. that are usually added to food may be appropriately blended as an optional ingredient, in addition to dried mulberry leaf which is an essential ingredient or an extract thereof it can. The food can be eaten in any form, liquid or solid. It can be eaten as a soft capsule encapsulated by gelatin or the like. The capsule is made of, for example, a gelatin film prepared by adding water to a raw material gelatin to dissolve, and adding a plasticizer (glycerin, D-sorbitol, etc.) thereto.
本発明の医薬品、薬剤においては、乾燥藍葉粉末または抽出物を単独で製剤として用いることができるほか、製薬上使用できる担体もしくは希釈剤を加えた製剤組成物に加工したものを用いることもできる。このような製剤または薬剤組成物は、経口または非経口の経路で投与することができる。例えば、経口投与用の固体または流体(ゲルおよび液体)の製剤または薬剤組成物は、タブレット、カプセル、錠剤、丸剤、粉末、顆粒もしくはゲル調製品の形態をとる。製剤または薬剤組成物の正確な投与量は、その目的とする使用形態および処置時間により変化するため、担当の医師または獣医が適当であると考える量になる。服用および投与用量は製剤形態によって適宜調整できる。錠剤などの経口固形製剤、経口液剤などとして1日服用量を1回ないし数回に分けて服用してもよい。また、例えばシロップやトローチ、チュアブル錠などの幼児頓服として、局所で作用させるとともに内服による全身性作用をも発揮させる製剤形態では1日服用量の1/2〜1/10を1回量として配合し服用すればよく、この場合全服用量が1日量に満たなくてもよい。
逆に、製剤形態からみて無理な服用容量とならなければ1日服用量に相当する量を1回分として配合してもよい。製剤の調製にあたっては、通常使用される充填剤、増量剤、結合剤、崩壊剤、表面活性剤、滑沢剤、コーティング剤、徐放化剤など、希釈剤や賦形剤を用いることができる。この他、必要に応じて溶解補助剤、緩衝剤、保存剤、可溶化剤、等張化剤、乳化剤、懸濁化剤、分散剤、増粘剤、ゲル化剤、硬化剤、吸収剤、粘着剤、弾性剤、可塑剤、吸着剤、香料、着色剤、矯味剤、抗酸化剤、保湿剤、遮光剤、光沢剤、帯電防止剤などを使用することができる。
In the pharmaceuticals and medicaments of the present invention, dry mulberry powder or extract can be used alone as a preparation, or it can be processed into a pharmaceutical composition to which a pharmaceutically usable carrier or diluent is added. Such formulations or pharmaceutical compositions can be administered by oral or parenteral routes. For example, solid or fluid (gel and liquid) formulations or pharmaceutical compositions for oral administration take the form of tablets, capsules, tablets, pills, powders, granules or gel preparations. The exact dose of the formulation or pharmaceutical composition will depend on the intended use and time of treatment, and so will be the amount deemed appropriate by the attending physician or veterinarian. The dose and administration dose can be appropriately adjusted depending on the form of preparation. As an oral solid preparation such as a tablet, an oral liquid preparation, etc., the daily dose may be taken once or several times. In addition, for example, in the form of a formulation that exerts a local action while exerting a systemic action by internal use, such as syrup, troche, chewable tablet, etc., 1/2 to 1/10 of the daily dose is formulated as a single dose The total dose may not be less than the daily dose.
On the contrary, if it does not become an unreasonable dose from the form of preparation, it may be blended as one dose equivalent to the daily dose. In preparation of the formulation, commonly used fillers, fillers, binders, disintegrants, surfactants, lubricants, coatings, sustained release agents, etc., diluents and excipients can be used. . In addition, if necessary, solubilizers, buffers, preservatives, solubilizers, isotonic agents, emulsifiers, suspending agents, dispersing agents, thickeners, gelling agents, curing agents, absorbents, A pressure-sensitive adhesive, an elastic agent, a plasticizer, an adsorbent, a fragrance, a coloring agent, a flavoring agent, an antioxidant, a moisturizing agent, a light shielding agent, a brightener, an antistatic agent and the like can be used.
本発明の乾燥藍葉に多く含まれるトリプタントリンの抗アレルギー作用、抗真菌作用を利用する皮膚外用剤、すなわち治療薬、皮膚外用剤、化粧料等が知られている肌荒れ、荒れ性に対して改善・予防効果を有する皮膚外用剤を提供することができる。本発明の皮膚外用剤には、乾燥藍葉または抽出物を必須成分とし、それ以外に、通常化粧品や医薬品等の皮膚外用剤に用いられる成分、例えば水性成分、油性成分、粉末成分、アルコール類、保湿剤、増粘剤、紫外線吸収剤、美白剤、防腐剤、酸化防止剤、界面活性剤、香料、色剤、各種皮膚栄養剤等を必要に応じて適宜配合することができる。その他、エデト酸二ナトリウム、エデト酸三ナトリウム、クエン酸ナトリウム、ポリリン酸ナトリウム、メタリン酸ナトリウム、グルコン酸等の金属封鎖剤、カフェイン、タンニン、ベラバミル、甘草抽出物、グラブリジン、カリンの果実の熱水抽出物、各種生薬、酢酸トコフェロール、グリチルリチン酸、トラネキサム酸およびその誘導体またはその塩等の薬剤、ビタミンC、アスコルビン酸リン酸マグネシウム、アスコルビン酸クルコシド、アルブチン、コウジ酸、D−グルコース、D−フルクトース、トレハロース等の糖類なども適宜配合することができる。本発明の皮膚外用剤は、例えば軟膏、クリーム、乳液、ローション、パック、浴用剤等、従来の皮膚外用剤に用いられる形態であればいずれでもよく、剤型は特に問わない。 The skin external preparation utilizing anti-allergic action and antifungal action of triptanthrin abundantly contained in dried mulberry leaves of the present invention, that is, a remedy, an external preparation for skin, a cosmetic preparation, etc. An external preparation for skin having a preventive effect can be provided. The external preparation for skin of the present invention contains a dry leaf or extract as an essential component, and in addition to the components generally used for external preparations for skin such as cosmetics and medicines, for example, aqueous components, oil components, powder components, alcohols, Moisturizers, thickeners, UV absorbers, skin lightening agents, preservatives, antioxidants, surfactants, perfumes, coloring agents, various skin nutrients and the like can be appropriately blended. Other sequestering agents such as disodium edetate, trisodium edetate, sodium citrate, sodium polyphosphate, sodium metaphosphate, gluconic acid, caffeine, tannin, verabamil, licorice extract, grubricin, heat of culin fruit Water extracts, various herbal medicines, drugs such as tocopherol acetate, glycyrrhizinic acid, tranexamic acid and derivatives thereof or salts thereof, vitamin C, magnesium ascorbate phosphate, curcoside ascorbic acid, arbutin, kojic acid, D-glucose, D-fructose Also, saccharides such as trehalose can be appropriately blended. The external preparation for skin of the present invention may be, for example, an ointment, a cream, an emulsion, a lotion, a pack, a bath preparation, etc., as long as it is used for conventional external preparations for skin.
藍顔料とする場合には、インジカン及び酵素を含む乾燥藍葉粉末を水に懸濁した後ろ過したろ液か、あるいは、それぞれの乾燥藍葉粉末の水抽出液をろ過してから混合した混合液に、タンパク質及び/または糖を加えてよく撹拌することにより、空気酸化によりインジゴを生成させ、タンパク質及び/または糖に生成したインジゴを吸着させるか、あるいはインジゴを凝集させることができる。その後、ろ過してから乾燥し、藍顔料を調製する。この藍顔料は、青色の着色料としてだけでなく、抗菌活性、抗アレルギー活性を有するトリプタントリンおよび神経活性物質であるイサチンが多く含まれているので、そのまま食する青色の機能性食品として、または石鹸、化粧品および抗菌、抗アレルギー、神経活性物質としての医薬品とすることが可能である。低酸素もしくは不活性ガス雰囲気下で同様の処理をすると、インジルビンを多く含む藍顔料の調製も可能である。 In the case of using as a pigment, a filtrate obtained by suspending dried indica powder containing indican and enzymes in water and then filtering, or a mixed solution obtained by filtering the water extract of each dried indica powder By adding protein and / or sugar and stirring well, it is possible to produce indigo by air oxidation, to adsorb the produced indigo to protein and / or sugar, or to aggregate indigo. After that, it is filtered and dried to prepare an amber pigment. This cocoon pigment is rich not only as a blue coloring agent but also with antibacterial activity, antiallergic activity, triptanthrin and the neuroactive substance isatin, so it can be eaten as it is as a blue functional food to be eaten as it is or It is possible to make soaps, cosmetics and medicines as antibacterial, antiallergic and neuroactive substances. The same treatment under a low oxygen or inert gas atmosphere also makes it possible to prepare indylbin-rich amber pigments.
特に、医薬品として用いる場合には、腸溶性物質で藍顔料をコーティングする工程を付加することにより藍顔料を製剤化すると、腸までそのままの状態で藍顔料を送達することができるので有効である。
腸溶性物質としては、小林ツエイン(小林香料(株))などの腸溶性タンパク質や、酢酸フタル酸セルロース、カルボキシメチルエチルセルロースなどのセルロース誘導体、メタクリル酸・アクリル酸エチル共重合体、ポリ酢酸フタル酸ビニル、ポリビニルアセテートフタル酸エステル、ヒプロメロースフタル酸エステルなどのポリマーを用いることができる。
In particular, when used as a pharmaceutical, it is effective to formulate the amber pigment by adding the step of coating the amber pigment with an enteric substance, since the amber pigment can be delivered as it is to the intestine, and this is effective.
Examples of enteric substances include enteric proteins such as Kobayashi Tuein (Kobayashi Fragrance Co., Ltd.), cellulose derivatives such as cellulose acetate phthalate and carboxymethyl ethyl cellulose, methacrylic acid / ethyl acrylate copolymer, polyvinyl acetate phthalate Polymers such as polyvinyl acetate phthalate and hypromellose phthalate can be used.
藍顔料の調製に使用するタンパク質としては、疎水性のタンパク質であれば、インジゴを吸着することができ、例えば、トウモロコシタンパク質のゼイン、小麦タンパク質のグルテン、牛乳由来のカゼインやラクトフェリンなどを用いる。添加するタンパク質の量は、多すぎると粘性が高くなり、インジゴの均一な沈着を阻害し、少なすぎると、タンパク質に吸着しないインジゴが増えることになる。 As a protein used for preparation of an amber pigment, indigo can be adsorbed if it is a hydrophobic protein, and for example, zein of corn protein, gluten of wheat protein, casein derived from milk, lactoferrin, etc. are used. When the amount of protein to be added is too large, the viscosity becomes high, and the uniform deposition of indigo is inhibited, and when it is too small, the amount of indigo not adsorbed to the protein is increased.
藍顔料の調製に使用する糖としては、疎水性、水溶性の糖のどちらも用いることができる。
疎水性の糖であればインジゴを吸着することができるが、β−シクロデキストリンが入手し易く便利である。添加する疎水性の糖の量は、多すぎると粘性が高くなり、インジゴの均一な沈着を阻害し、少なすぎると、タンパク質に吸着しないインジゴが増えることになる。
Both hydrophobic and water-soluble sugars can be used as sugars used for the preparation of amber pigments.
Although hydrophobic sugars can adsorb indigo, β-cyclodextrin is easily accessible and convenient. When the amount of hydrophobic sugar to be added is too large, the viscosity becomes high, and the uniform deposition of indigo is inhibited, and when it is too small, the amount of indigo which is not adsorbed to protein increases.
水溶性の糖は、インジゴを吸着できない代わりに、インジカン溶液に添加すると、酵素作用により生成されたインジゴを沈降させ、凝集させることができる。例えば、グルコース、ショ糖、α−シクロデキストリン等をインジカン溶液に添加すると、水溶性の糖が凝集剤の役割を果たして、生成したインジゴが沈降する。この酵素は高い糖濃度でも安定であるため、0.5%〜20%の糖濃度でもインジゴの生成反応が進行するが、糖の添加量が多すぎると粘性が高くなるので、1〜5%の糖濃度になるように糖を添加するとよい。 Instead of being unable to adsorb indigo, water soluble sugars can be added to the indican solution to precipitate and aggregate indigo produced by the enzymatic action. For example, when glucose, sucrose, α-cyclodextrin and the like are added to the indican solution, the water-soluble sugar acts as a flocculant, and the generated indigo precipitates. Since this enzyme is stable even at high sugar concentrations, the indigo generation reaction proceeds even at sugar concentrations of 0.5% to 20%, but if the amount of sugar added is too high, the viscosity increases, so 1 to 5% It is good to add sugar so that it may become sugar concentration.
また、マイクロ波熟成乾燥藍葉、または、水および/または溶媒で抽出した抽出物には青色でないが、抗菌活性、抗アレルギー活性を有するトリプタントリンや神経活性物質であるイサチンが高濃度で含有されている。よって、高機能性乾燥藍葉またはその抽出物は、機能性食品素材、化粧品素材および抗菌、抗アレルギー、またはパーキンソン病等に効果のある神経活性物質としての医薬品素材(原料)として使用できる。 In addition, microwave-ripened dried mulberry leaves or extracts extracted with water and / or solvent do not have a blue color, but contain high concentrations of tryptanthrin having an antibacterial activity and an antiallergic activity, and a neuroactive substance isatin. There is. Therefore, the highly functional dry mulberry leaf or its extract can be used as a functional food material, a cosmetic material and a pharmaceutical material (raw material) as a neuroactive substance effective for antibacterial, antiallergic or Parkinson's disease and the like.
乾燥藍葉、または、水および/または溶媒で抽出した抽出物を飲食品用、化粧品用、医薬品用に用いることは、すべて公知の用途であり、マイクロ波熟成乾燥藍葉に機能性成分が多いことを考慮する以外は、同様に普通の使い方がなされる。医薬品の場合、カプセルや粉末、錠剤などとして経口投与することができ、投与量は症状の度合いや体重、年齢、性別などにより異なるものであり、使用に際して適当な量を症状に応じて決めることが望ましい。医薬品における配合量は特に制限はされないが、なお、本発明の藍葉は漢方薬の原料として用いられており、安全性が高いものである。 The use of dried mulberry leaves or extracts extracted with water and / or solvent for food and drink, cosmetics and pharmaceuticals is all known use, and there are many functional ingredients in microwave ripening dried mulberry leaves The usual usage is the same except for consideration. In the case of pharmaceuticals, they can be orally administered as capsules, powders, tablets and the like, and the dosage varies depending on the degree of symptoms, body weight, age, sex, etc. desirable. The compounding amount in the pharmaceutical is not particularly limited, but the mulberry leaves of the present invention are used as a raw material of traditional Chinese medicine, and are highly safe.
本発明の機能性食品は、特定の疾病などを予防する健康食品、予防医薬品の分野の利用に適している。特定の疾病を予防する健康食品においては、必須成分である乾燥藍葉またはその抽出物の他に、任意的成分として、通常食品に添加されるビタミン類、炭水化物、色素、香料など適宜配合することができる。食品は液状または固形の任意の形態で食することができる。ゼラチンなどで外包してカプセル化した軟カプセル剤として食することができる。 The functional food of the present invention is suitable for use in the fields of health food and preventive medicine that prevent specific diseases and the like. In health foods that prevent specific diseases, vitamins, carbohydrates, pigments, flavors, etc. that are usually added to food may be appropriately blended as an optional ingredient, in addition to dried mulberry leaf which is an essential ingredient or an extract thereof it can. The food can be eaten in any form, liquid or solid. It can be eaten as a soft capsule encapsulated by gelatin or the like.
本発明の医薬品、薬剤においては、出願前公知の通常の使用態様を含み、乾燥藍葉粉末または抽出物を単独で製剤として用いることができるほか、製薬上使用できる担体もしくは希釈剤を加えた製剤組成物に加工したものを用いることもできる。このような製剤または薬剤組成物は、経口または非経口の経路で投与することができる。製剤または薬剤組成物の正確な投与量は、その目的とする使用形態および処置時間により変化するため、担当の医師または獣医が適当であると考える量になる。服用および投与用量は製剤形態によって適宜調整できる。 The pharmaceutical composition of the present invention includes the usual usage mode known prior to the application, and a dry mulberry powder or extract can be used alone as a formulation, and a pharmaceutical composition containing a pharmaceutically usable carrier or diluent What was processed into a thing can also be used. Such formulations or pharmaceutical compositions can be administered by oral or parenteral routes. The exact dose of the formulation or pharmaceutical composition will depend on the intended use and time of treatment, and so will be the amount deemed appropriate by the attending physician or veterinarian. The dose and administration dose can be appropriately adjusted depending on the form of preparation.
本発明の乾燥藍葉に多く含まれるトリプタントリンの抗アレルギー作用、抗真菌作用を利用する皮膚外用剤、すなわち治療薬、皮膚外用剤、化粧料等が知られている。肌荒れ、荒れ性に対して改善・予防効果を有する皮膚外用剤を提供することができる。本発明の皮膚外用剤には、乾燥藍葉または抽出物を必須成分とし、それ以外に、通常化粧品や医薬品等の皮膚外用剤に用いられる成分、例えば水性成分、油性成分、粉末成分、アルコール類、保湿剤、増粘剤、紫外線吸収剤、美白剤、防腐剤、酸化防止剤、界面活性剤、香料、色剤、各種皮膚栄養剤等を必要に応じて適宜配合することができる。本発明の皮膚外用剤は、例えば軟膏、クリーム、乳液、ローション、パック、浴用剤等、従来の皮膚外用剤に用いられる形態であればいずれでもよく、剤型は特に問わない。 The skin external preparation which utilizes the antiallergic action and antifungal action of triptanthrin abundantly contained in the dried mulberry leaves of the present invention, that is, a therapeutic agent, a skin external preparation, a cosmetic and the like are known. It is possible to provide an external preparation for skin having an improving and preventing effect on rough and rough skin. The external preparation for skin of the present invention contains a dry leaf or extract as an essential component, and in addition to the components generally used for external preparations for skin such as cosmetics and medicines, for example, aqueous components, oil components, powder components, alcohols, Moisturizers, thickeners, UV absorbers, skin lightening agents, preservatives, antioxidants, surfactants, perfumes, coloring agents, various skin nutrients and the like can be appropriately blended. The external preparation for skin of the present invention may be, for example, an ointment, a cream, an emulsion, a lotion, a pack, a bath preparation, etc., as long as it is used for conventional external preparations for skin.
図2は、本発明に係るマイクロ波加熱装置の構成図である。この装置は、特許文献3に記載の装置と同様のハードウェア構成であり、加熱容器と、加熱容器の蓋とから構成される加熱釜を備えている。加熱容器および蓋は、それぞれフランジ部を有しており、対向する両フランジ部を狭圧することにより固定される。加熱釜は、例えば、数リットル〜数百リットルの容量(最低容量は撹拌羽根の中央固定ノブが隠れる液量、最大容量は攪拌時の液面上昇を加味すれば、釜容量の2/3となる)であり、複数の加熱釜を連結して使用する場合もある。乾燥時、抽出時およびブランチング時には、気化効率を高めるために加熱釜内を減圧する。
加熱容器には、排水バルブが設けられた配管および駆動装置が接続される。駆動装置は、例えばモータであり、接続軸を介して撹拌羽根を回動させる。
FIG. 2 is a block diagram of a microwave heating apparatus according to the present invention. This device has the same hardware configuration as the device described in Patent Document 3, and includes a heating pot including a heating container and a lid of the heating container. The heating container and the lid each have a flange and are fixed by narrowing the opposing flanges. The heating kettle has, for example, a volume of several liters to several hundred liters (the minimum volume is the amount of liquid that hides the central fixing knob of the stirring blade, and the maximum volume is 2/3 of the volume of the kettle if the liquid level rise during stirring is taken into account). In some cases, a plurality of heating pots may be connected and used. During drying, extraction and blanching, the pressure in the heating kettle is reduced in order to increase the vaporization efficiency.
The heating container is connected to a pipe provided with a drainage valve and a drive unit. The drive device is, for example, a motor, and rotates the stirring blade via the connection shaft.
蓋には、導波管および大気開放バルブが設けられた配管が接続される。大気開放バルブは、圧力逃し弁(ベント)として機能するものであるが、必須の構成ではない。 The lid is connected to a pipe provided with a waveguide and an atmosphere release valve. The atmosphere release valve functions as a pressure relief valve (vent) but is not an essential component.
温度センサは、容器の内容物の温度を測定する接触型の光ファイバー型温度センサである。光ファイバー型温度センサの感温部である先端にはアルミナ製あるいはガラス製の保護管が被せられ、保護管を容器に挿入される。光ファイバー型温度センサは、光検出器と接続されており、光検出器が測定した温度に基づきマイクロ波発振器の出力が制御される。
例示の光ファイバー型温度センサに代え、或いは、光ファイバー型温度センサと共に放射型温度センサを設けてもよい。放射型温度センサは、例えば、赤外線や可視光線の強度を測定する非接触型の温度センサである。
The temperature sensor is a contact type optical fiber temperature sensor that measures the temperature of the contents of the container. A protective tube made of alumina or glass is covered on the tip of the temperature sensor of the optical fiber type temperature sensor, and the protective tube is inserted into the container. The fiber optic temperature sensor is connected to the light detector, and the output of the microwave oscillator is controlled based on the temperature measured by the light detector.
A radiant temperature sensor may be provided instead of the illustrated optical fiber temperature sensor, or together with the optical fiber temperature sensor. The radiation type temperature sensor is, for example, a noncontact temperature sensor that measures the intensity of infrared light or visible light.
導波管が接続される蓋の開口部には、マイクロ波を吸収しないマイクロ波透過性材からなる照射窓(図示せず)を設けることが好ましい。この照射窓は、例えば、石英、セラミックス、テフロン(登録商標)などにより構成することができる。導波管の接続位置は図示する空間照射の態様に限定されず、液中照射するものでもよい。また、導波管は、複数本設けてもよく、空間照射と液中照射を組み合わせてもよい。 In the opening of the lid to which the waveguide is connected, it is preferable to provide an irradiation window (not shown) made of a microwave transmitting material that does not absorb microwaves. The irradiation window can be made of, for example, quartz, ceramics, Teflon (registered trademark) or the like. The connection position of the waveguide is not limited to the illustrated mode of space irradiation, and may be in-liquid irradiation. In addition, a plurality of waveguides may be provided, and spatial irradiation and in-liquid irradiation may be combined.
導波管の蓋とは逆側の端部は、マイクロ波発振器と接続されている。マイクロ波発振器は、制御装置と信号線で接続されており、制御装置からの制御信号(例えば、デューティ制御またはPWM制御)に基づいてマイクロ波を照射するマイクロ波源(例えば、マグネトロンまたは半導体発振器)を備えている。制御装置は、演算装置と、温度センサからの信号に基づき本発明のマイクロ波熟成乾燥藍葉の製造方法を実行するための制御プログラムが格納された記憶装置とを備えている。
熟成は低出力のマイクロ波(例えば、1L容器であれば10〜50Wでの連続照射相当、100L容器であれば1〜5kWでの連続照射相当)で行う必要があるところ、マイクロ波源に半導体発振器を使えば、低出力で安定した発信が可能となる。マイクロ波源がマグネトロンの場合、デューティまたはPWM制御をすることで、低温で安定した制御が可能となる。例えば、1.5kWのマグネトロンの最大出力を15%に制限し、デューティ比を20%で出力すれば、マイクロ波出力は連続照射時の45Wに相当する(1.5kWのマグネトロンを用いて45Wで安定的に連続照射することはできない。)。
The end of the waveguide opposite to the lid is connected to a microwave oscillator. The microwave oscillator is connected to the control device by a signal line, and a microwave source (for example, a magnetron or a semiconductor oscillator) which emits a microwave based on a control signal (for example, duty control or PWM control) from the control device. Have. The control device includes an arithmetic device, and a storage device storing a control program for executing the method for producing microwave-ripened dried leaves according to the present invention based on a signal from a temperature sensor.
Aging should be performed by low power microwave (for example, continuous irradiation equivalent to 10 to 50 W for 1 L container, equivalent to continuous irradiation for 1 to 5 kW for 100 L container). Enables stable transmission with low output. When the microwave source is a magnetron, stable control at low temperature is possible by performing duty or PWM control. For example, if the maximum output of a 1.5 kW magnetron is limited to 15% and the duty ratio is output at 20%, the microwave output corresponds to 45 W during continuous irradiation (45 W using a 1.5 kW magnetron It is not possible to stably irradiate continuously.)
以下、本発明の詳細を実施例に基づき説明するが、本発明はこれらの実施例により何ら限定されない。 The details of the present invention will be described below based on examples, but the present invention is not limited at all by these examples.
乾燥藍葉粉末に含まれるインジカン分解酵素の酵素活性と各染色成分等の濃度を、以下の測定方法、測定キットを用いて測定する。 The enzyme activity of the indican degradation enzyme contained in the dried mulberry leaf powder and the concentration of each staining component and the like are measured using the following measurement method and measurement kit.
[酵素活性測定]
乾燥葉抽出液のβ−グルコシダーゼ活性(インジカン分解酵素活性)は、以下の手順で測定する。測定値は、3回の平均値を求めて結果の値とした(n=3)。
(1)乾燥葉粉末0.5gにイオン精製水40mlを加え、室温で3時間以上撹拌し、藍葉抽出液を得る。
[Enzyme activity measurement]
The β-glucosidase activity (indicane degrading enzyme activity) of the dried leaf extract is measured according to the following procedure. The measured value was determined as the value of the result obtained by averaging three times (n = 3).
(1) 40 ml of ion-purified water is added to 0.5 g of dried leaf powder, and the mixture is stirred at room temperature for 3 hours or more to obtain a mulberry leaf extract.
(2)p-ニトロフェニル β-D-グルコピラノシド(β-NPG)75.31mgにイオン精製水を加えて10mlにして25mM β-NPG溶液を調製する。
(3)25mM β-NPG基質水溶液8μlを200μlのバッファー溶液に溶かして基質反応溶液を調製する。
(2) Ion-purified water is added to 75.31 mg of p-nitrophenyl β-D-glucopyranoside (β-NPG) to make it 10 ml to prepare a 25 mM β-NPG solution.
(3) Dissolve 8 μl of 25 mM β-NPG substrate aqueous solution in 200 μl of buffer solution to prepare a substrate reaction solution.
(4)測定試料は、ウエルに20μl注入し、基質反応溶液200μlを加える。陽性対照試料は、イオン精製水20μlに、タートラジンからなる標準溶液10ml(250U/L相当)200μlを加える。陰性対照試料は、イオン精製水220μlをウエルに注入する。 (4) 20 μl of the measurement sample is injected into the well, and 200 μl of the substrate reaction solution is added. As a positive control sample, 200 μl of a standard solution consisting of tartrazine (corresponding to 250 U / L) is added to 20 μl of ion-purified water. For negative control samples, inject 220 μl of ion-purified water into the wells.
(5)加える試料と試薬類を37℃でインキュベーションしておき、各試料をウエルに仕込んだ後(37℃)、マイクロプレートリーダーを用いて、0分後と20分後の吸光度(405nm)を測定する。 (5) Incubate the samples and reagents to be added at 37 ° C, load each sample into the wells (37 ° C), and then use the microplate reader to measure the absorbance (405 nm) after 0 and 20 minutes. taking measurement.
(6)20分後のODから0分後のODを差し引いた値を、陽性対照試料のODから陰性対照試料のODを差し引いた値で割り、250(U/L)を掛けた値が、酵素活性値(U/L)となる。酵素活性値(U/kg)は、酵素活性値(U/L)に80を乗じて計算する。 (6) The value obtained by subtracting the OD after 0 min from the OD after 20 min is divided by the OD of the positive control sample minus the OD of the negative control sample and multiplied by 250 (U / L). It becomes an enzyme activity value (U / L). The enzyme activity value (U / kg) is calculated by multiplying the enzyme activity value (U / L) by 80.
[染色成分等の定量]
乾燥葉に含まれる染色成分は、乾燥葉粉末0.5gに、DMSO 40mlを加え、MW出力500W、60℃、15分間撹拌して抽出する。得られた抽出液をシリンジフィルターでろ過し、インジカン、イチサン、インジゴ、インジルビン、トリプタトリンのHPLC分析による定量を行う。
[Quantification of staining components etc.]
The dye components contained in the dried leaves are extracted by adding 40 ml of DMSO to 0.5 g of dried leaf powder and stirring for 15 minutes at a MW output of 500 W at 60 ° C. for 15 minutes. The resulting extract is filtered through a syringe filter and quantified by HPLC analysis of indican, itisan, indigo, indirubin, triptatriline.
HPLC分析では、Inertsil ODS-3Vカラムを使用する。溶離液は、アセトニトリル水溶液を40℃、1.0ml/分の流量で流す。溶離液のグラジエントプログラムは、15%(0分);85%(15分);85%(20分)である。測定波長は、インジカン測定時に215〜230nm、イサチン、インジゴ、インジルビン、トリプタントリン測定時に290〜310nmを使用する。 For HPLC analysis, use an Inertsil ODS-3V column. As the eluent, acetonitrile aqueous solution is flowed at 40 ° C. and a flow rate of 1.0 ml / min. The gradient program of the eluent is 15% (0 minutes); 85% (15 minutes); 85% (20 minutes). The measurement wavelength is 215 to 230 nm in indican measurement, and 290 to 310 nm in isatin, indigo, indirubin, and triptanthrin measurement.
水耕栽培していたタデ藍の品種「千本」を刈り取りって、藍葉の軸を取ってから脱水のためによく水切りした。その生藍葉を、(1)室内でそのまま数日間乾燥した(自然乾燥葉)、(2)定温乾燥機に入れ、40℃で1〜2日乾燥した(定温乾燥葉)、(3)図2(特許文献3)に記載の撹拌機能付の大量処理のできるマイクロ波照射装置(四国計測工業株式会社製)に入れ、40℃で30分間0.09MPaの減圧下でマイクロ波を照射して熟成し、マイクロ波減圧乾燥により葉の重量を約60%減少させた後、定温乾燥機に入れ40℃で乾燥した(マイクロ波熟成乾燥葉)。 The variety "Senbon", which is a cultivar of Tade mushroom that had been hydroponically cultivated, was harvested and the stems of mulberry leaves were taken and then drained well for dehydration. The ginger leaf was (1) dried in the room as it was for several days (naturally dried leaf), (2) placed in a constant temperature drier and dried at 40 ° C. for 1 to 2 days (constant temperature dried leaf), (3) FIG. It is put in the microwave irradiation device (made by Shikoku Measurement Industry Co., Ltd.) capable of mass treatment with stirring function described in (Patent Document 3), and it is aged by irradiating the microwave under reduced pressure of 0.09 MPa for 30 minutes at 40 ° C The leaf weight was reduced by about 60% by microwave vacuum drying, and then placed in a constant temperature drier and dried at 40 ° C. (microwave ripened dry leaf).
これら3種類の乾燥葉を、それぞれピンミルで粉砕し、粉末化した乾燥葉粉末0.5gにイオン精製水40mlを加え、室温で3時間以上撹拌し、藍葉抽出液を得、抽出液中の酵素活性を測定した。また、3種類の乾燥粉末の一定量にそれぞれDMSOを加えて、マイクロ波法で溶解し、各乾燥葉に含まれるトリプタントリンの濃度をHPLCで分析した。乾燥藍葉粉末中の酵素活性(U/kg)とトリプタントリンの濃度(ppm)の測定結果を表1に示す。 These three types of dried leaves were each crushed with a pin mill, 40 ml of ion-purified water was added to 0.5 g of powdered dried leaf powder, and stirred at room temperature for 3 hours or more to obtain an extract of mulberry leaves, enzymes in the extract Activity was measured. In addition, DMSO was added to each of a fixed amount of three types of dry powders, each was dissolved by a microwave method, and the concentration of triptanthrin contained in each dry leaf was analyzed by HPLC. The measurement results of the enzyme activity (U / kg) and the concentration of triptanthrin (ppm) in the dry mulberry leaf powder are shown in Table 1.
マイクロ波熟成乾燥葉のインジカン分解酵素活性は、自然乾燥葉の14倍高くなっており、トリプタントリン濃度も、自然乾燥葉および定温乾燥葉の10倍以上高くなっていた。 The indican degradation enzyme activity of microwave ripened dry leaves was 14 times higher than that of natural dry leaves, and the triptanthrin concentration was also 10 times higher than that of natural dry leaves and isothermal dry leaves.
マイクロ波熟成乾燥葉の酵素活性、トリプタントリン濃度が、自然乾燥葉や定温乾燥葉のものに比べて大幅に増加することがわかった。次に、生藍葉に傷をつけたり、マイクロ波熟成乾燥の条件や使用するマイクロ波照射装置により、酵素活性、トリプタントリン濃度、さらには、インジカン、イサチン、インジゴ、インジルビン濃度がどのように変化するかについて実験した。 It was found that the enzyme activity and tryptanthrin concentration of microwave-ripened dry leaves were significantly increased as compared to those of natural dry leaves and isothermal dry leaves. Next, how the enzyme activity, tryptanthrin concentration, and further the indican, isatin, indigo and indirubin concentration change depending on the condition of microwave ripening and drying and the microwave irradiation equipment used to damage the ginger leaf or conditions of microwave ripening and drying It experimented about.
刈り取った藍葉の軸を取ってから、脱水のためによく水切りした。対照は、自然乾燥のみの室温乾燥(比較例1)とした。 After harvesting the stems of the harvested mulberry leaves, it was drained well for dehydration. The control was room temperature drying (comparative example 1) with only natural drying.
まず、マイクロ波照射装置として、撹拌機能のないキャビティ型装置(SMW107、最大出力1.5kw)を用い、キャビティ内に1〜2lの容量のガラス容器を入れて、その中に50gほどの生藍葉と若干量の水を入れてマイクロ波照射した。温度40℃のマイクロ波照射による熟成時間と40〜45℃のマイクロ波減圧乾燥による加熱時間を変化させた。加熱後の乾燥は、40℃の定温乾燥で行った(実験例1〜6)。
水耕藍葉の品種千本を、水耕場所の3つの異なる場所から刈り取った。(水耕1〜3)
実験例1 水耕1の藍葉、熟成 15分、加熱 20分
実験例2 水耕1の藍葉、熟成 30分、加熱 20分
実験例3 水耕2の藍葉、熟成 30分、加熱 なし
実験例4 水耕2の藍葉、熟成 30分、加熱 20分
実験例5 水耕3の藍葉、熟成 60分、加熱 10分
実験例6 水耕3の藍葉、熟成 30分、加熱 7分
比較例1 水耕1の藍葉 室温乾燥
First, using a cavity type device without a stirring function (SMW 107, maximum output 1.5 kw) as a microwave irradiation device, a glass container with a capacity of 1 to 2 liters is placed in the cavity, and about 50 g of ginger leaf And microwaved with some water. The aging time by microwave irradiation at a temperature of 40 ° C. and the heating time by microwave reduced-pressure drying at 40-45 ° C. were changed. Drying after heating was performed by constant temperature drying at 40 ° C. (Experimental Examples 1 to 6).
One thousand varieties of hydroponic mulberry leaves were harvested from three different locations of the hydroponic location. (Water culture 1 to 3)
EXPERIMENTAL EXAMPLE 1 Mulberry leaves in water culture 1, ripening 15 minutes, heating 20 minutes Experimental example 2 Mulberry leaves in water culture 1, ripening 30 minutes, heating 20 minutes Experimental example 3 Mulberry leaves in water culture 2, ripening 30 minutes, heating none Experimental example 4 Mulberry leaves in water culture 2, aging 30 minutes, heating 20 minutes Experimental example 5 Mulberry leaves in water culture 3, ripening 60 minutes, heating 10 minutes Experimental example 6 Mulberry leaves in water culture 3, ripening 30 minutes, heating 7 minutes Comparative example 1 water culture 1 mulberry leaves room temperature drying
次に、図2(特許文献3)に記載の撹拌機能付の大量処理のできるマイクロ波照射装置(四国計測工業株式会社製)を用いた。容量が最大160lの釜の中に直接マイクロ波を照射でき、1回の処理で生藍葉4〜5kgをマイクロ波処理可能であり、最大出力は、18kWである。 Next, a microwave irradiation apparatus (manufactured by Shikoku Measuring Industry Co., Ltd.) capable of performing a large amount of processing with a stirring function described in FIG. 2 (Patent Document 3) was used. Microwave can be irradiated directly into the kettle with a maximum capacity of 160 l, and 4-5 kg of ginger leaves can be microwave-processed in one treatment, and the maximum output is 18 kW.
刈り取った生藍葉の軸を取って水切りした後、藍葉はザルに2、3kg入れて多段にセットし、12rpmでゆっくり回転させながら、36〜40℃の温度で30分間マイクロ波照射して熟成させた。熟成後、40〜45℃で0.01MPaの減圧下でマイクロ波減圧乾燥させた後、定温乾燥機に入れて40℃で乾燥した。実験例7〜10は、同じ条件で日を変えて4回マイクロ波熟成乾燥させたものである。 After removing the stem of the cut ginger leaf and draining it, put 2-3 kg into the monkey and set it in multiple stages, aging it by microwave irradiation at temperature of 36-40 ° C for 30 minutes while rotating slowly at 12 rpm The After ripening, microwave drying was carried out at 40-45 ° C. under a reduced pressure of 0.01 MPa, and then it was placed in a constant temperature drier and dried at 40 ° C. Experimental Examples 7 to 10 were subjected to microwave ripening and drying four times at different conditions under the same conditions.
比較例2は、熟成なしで、40〜45℃で0.01MPaの減圧下でマイクロ波減圧乾燥させた後、定温乾燥機に入れて40℃で乾燥したものである。 Comparative Example 2 is one obtained by microwave drying under reduced pressure of 0.01 MPa at 40 to 45 ° C. without aging, and then drying at 40 ° C. by placing in a constant temperature dryer.
実験例11は、刈り取った藍葉の軸を取ってから、脱水のためによく水切りして、カッターでみじん切りにしてから、実験例7〜10と同じ条件で、熟成乾燥させたものである。 Experimental Example 11 is obtained by taking the stems of cut mulberry leaves, draining well for dehydration, mincing with a cutter, and then ripening and drying under the same conditions as Experimental Examples 7 to 10.
実験例1〜11および比較例1、2の乾燥藍葉の、酵素活性、トリプタントリン、インジカン、イサチン、インジゴ、インジルビン濃度は、以下の表2のとおりである。 The enzyme activity, tryptanthrin, indican, isatin, indigo and indirubin concentrations of dried mulberry leaves of Experimental Examples 1 to 11 and Comparative Examples 1 and 2 are as shown in Table 2 below.
実験例1〜10では、比較例1、2に比べ、インジカン分解酵素活性が1.3倍以上高くなり、特に、撹拌機能付の大量に処理できるマイクロ波照射装置を使用すると、酵素活性が顕著に高まった。インジカン分解酵素活性は、室温乾燥のものの1040(U/kg)に比べ、1389〜13851(U/kg)にもなっており、1.3倍から13倍以上高くなっている。また、トリプタントリンおよびイサチンを合成する酵素の活性も高まったことから、実験例7〜10ではトリプタントリン濃度は、熟成工程のない比較例2の245(ppm)に比べ、376〜2124(ppm)になっており、1.5倍から9倍高くなっている。 In Experimental Examples 1 to 10, the indican degradation enzyme activity is 1.3 times or more higher than in Comparative Examples 1 and 2, and the enzyme activity is remarkable particularly when using a microwave irradiation apparatus capable of treating a large amount with a stirring function. Increased. The indican degrading enzyme activity is as high as 1389 to 13851 (U / kg) as compared with 1040 (U / kg) of room temperature drying, and is 1.3 to 13 times higher than that. In addition, since the activities of enzymes that synthesize tryptanthrin and isatin were also enhanced, in experimental examples 7 to 10, the tryptanthrin concentration was 376 to 2124 (ppm) compared to 245 (ppm) of comparative example 2 without the ripening step. It is 1.5 times to 9 times higher.
同様に、イサチン濃度も実験例1〜11の全てで、顕著に高くなる。比較例1の56(ppm)に比べ、283〜3688(ppm)と高くなり、5倍から66倍高くなる。その結果、インジカンが酵素分解されたインドキシルが酸化されて生成されるインジゴおよびイサチンの量比も変化し、インジゴ濃度/イサチン濃度は、比較例1の自然乾燥葉では112であるのに対して、実験例1〜11では、いずれも40以下となっている。図1は、インジゴ濃度/イチサン濃度を縦軸にして、実験例の番号を横軸に示したものである。比較例1を室温乾燥としてプロットした。
また、実験例11のように、生藍葉にみじん切り等の物理的処理を施して藍葉を傷つけてから熟成すると、酵素活性がより高まることが確認された。
Similarly, the isatin concentration also increases significantly in all of Experimental Examples 1-11. Compared to 56 (ppm) of Comparative Example 1, it is as high as 283 to 3688 (ppm) and 5 to 66 times as high. As a result, the ratio of indigo and isatin, which is produced by oxidation of indoxyl in which the indican is enzymatically degraded, is also changed, and the indigo concentration / isatin concentration is 112 in the naturally dried leaves of Comparative Example 1 In the experimental examples 1 to 11, all are 40 or less. FIG. 1 shows the numbers of the experimental examples on the horizontal axis, with the indigo concentration / itisan concentration on the vertical axis. Comparative Example 1 was plotted as room temperature drying.
In addition, it was confirmed that the enzyme activity is further enhanced when physical properties such as mincing are applied to ginger leaves to damage the mulberry leaves and then ripening as in Experimental Example 11.
生藍葉として、露地栽培の品種「小上粉」を使用した。刈り取った藍葉をよく洗って軸をとり、脱水のためによく水切りした。実施例2と同様に、藍葉はザルに2.3kg入れて多段にセットし、12rpmでゆっくり回転させながら、36〜40℃の温度で30分間マイクロ波照射して熟成させた。熟成後、40〜45℃で0.01MPaの減圧下でマイクロ波減圧乾燥させた後、定温乾燥機に入れて40℃で乾燥した。対照として、熟成なしで、40〜45℃で0.01MPaの減圧下でマイクロ波減圧乾燥させた後、定温乾燥機に入れて40℃で乾燥した。
マイクロ波照射により熟成させた乾燥藍葉粉末中の酵素活性は、対照のものより高く、トリプタントリン濃度も高かった。
As a ginger leaf, the variety "Kogami flour" of open field cultivation was used. The cut mulberry leaves were washed well, the stem was taken and drained well for dehydration. In the same manner as in Example 2, 2.3 kg of mulberry leaves were placed in a monkey and set in multiple stages, and aged by microwave irradiation at a temperature of 36 to 40 ° C. for 30 minutes while slowly rotating at 12 rpm. After ripening, microwave drying was carried out at 40-45 ° C. under a reduced pressure of 0.01 MPa, and then it was placed in a constant temperature drier and dried at 40 ° C. As a control, it was microwave-reduced under reduced pressure of 0.01 MPa at 40-45 ° C. without aging, and then placed in a constant temperature dryer and dried at 40 ° C.
The enzyme activity in the dried mulberry leaf powder aged by microwave irradiation was higher than that of the control, and the triptanthrin concentration was also high.
生葉として水耕栽培「千本」を、マイクロ波減圧乾燥装置を使用し、藍葉を前処理なしで、5kPa以下、30℃で迅速乾燥した。実験aは採取したものを常温で運搬、そのままマイクロ波減圧乾燥したものである。実験bは藍葉を採取した後、氷を上に載せて運搬し、乾燥したものである。実験cはマイクロ波を大気圧下で照射し、85℃、5分間加熱ブランチング処理したものである。実験dはマイクロ波を照射して大気圧下85℃、5分加熱ブランチングしたものに、ブランチング処理葉に、1/5量の生葉を加え、5kPa、30℃で迅速乾燥したものである。いずれの場合もマイクロ波減圧乾燥で60〜70%の水分を回収した後、40℃で定温乾燥したものである。インジカン等の分析結果を表3に示す。 Hydroponics "Senmoto" as fresh leaves was rapidly dried at 30 ° C. or less at 5 ° C. or less using a microwave reduced-pressure drying apparatus and without pretreatment of mulberry leaves. In experiment a, the collected product was transported at room temperature and was subjected to microwave vacuum drying as it was. In Experiment b, after collecting mulberry leaves, ice was placed on top, transported and dried. In experiment c, microwaves were irradiated at atmospheric pressure and heat blanched at 85 ° C. for 5 minutes. In Experiment d, 1/5 amount of fresh leaves were added to blanched leaves after blanched at 85 ° C. for 5 minutes under microwave pressure and heated for 5 minutes, and rapidly dried at 5 ° C. and 30 ° C. . In any case, after 60 to 70% of the water content is recovered by microwave reduced pressure drying, constant temperature drying is performed at 40 ° C. The analysis results of indican etc. are shown in Table 3.
実験aは藍葉を採取した後、前処理なしで5kPa以下、30℃の条件で迅速乾燥したが、インジカンはほぼなく分解され、検出できなかった。実験bの藍葉を採取後、氷の入った保冷箱にいれて運搬して、保冷箱から出して直ぐ、5kPa、30℃の条件でマイクロ波蒸留乾燥した。インジカン濃度はかなり減少したが、1/5程度残っていた。インジルビン濃度がかなり高くなった。実験cは、マイクロ波ブランチング処理したものである。すなわち、大気圧下、マイクロ波を照射して85℃、5分間処理して、酵素を失活させた後、成分濃度を分析した結果、インジカン濃度が高く、インジゴの生成量は1/10程度であった。実験dは藍葉をブランチング処理(85℃、5分)したものに、生の藍葉を添加し、混ぜ合わせたのち、5kPa、30℃でマイクロ波減圧乾燥した。インジカンがほぼ残っており、生成したインジゴが少なく、その他の成分もほとんど生成しないことが分かった。なおこの粉末乾燥葉を水でペースト状にして毛束を処理した結果、良好に染毛できた。 In Experiment a, after collecting mulberry leaves, rapid drying was carried out under conditions of 5 kPa or less at 30 ° C. without pretreatment, but the indican was almost completely decomposed and could not be detected. After the mulberry leaves of Experiment b were collected, they were transported in a cold box containing ice and immediately removed from the cold box, and microwave distillation drying was performed under the conditions of 5 kPa and 30 ° C. Although the concentration of indican decreased considerably, it remained about 1/5. The indirubin concentration was considerably higher. Experiment c is a microwave blanching process. That is, after irradiating microwaves under atmospheric pressure and treating at 85 ° C. for 5 minutes to inactivate the enzyme, the concentration of the component was analyzed. As a result, the indican concentration is high, and the amount of indigo produced is about 1/10. Met. In Experiment d, raw mulberry leaves were added to those obtained by blanching the mulberry leaves (85 ° C., 5 minutes), mixed, and then dried under reduced pressure at 5 kPa and 30 ° C. under microwaves. It was found that the indican almost remained, generated less indigo and hardly generated other components. In addition, as a result of processing the hair bundle by making this powder dry leaf into a paste form and processing a hair bundle, it was able to be dyed favorably.
水耕栽培藍葉「千本」を採取した後、マイクロ波減圧乾燥前に、ブドウ糖、砂糖、酒の粕、次亜塩素酸の1%程度の水溶液に藍葉を10分程度浸漬した後、5kPa、30℃以下で迅速マイクロ波減圧蒸留乾燥した。インジカン等の分析結果を表4に示す。 After collecting the water culture cultivation mulberry leaves "Senjyo", after soaking the mulberry leaves in an aqueous solution of about 1% of glucose, sugar, sake lees, hypochlorous acid for about 10 minutes before microwave decompression drying, 5 kPa, 30 Rapid microwave vacuum distillation drying below ° C. The analysis results of indican etc. are shown in Table 4.
マイクロ波減圧乾燥する前に、酵素の働きを鈍くすることを目的に各種の水溶液に浸漬し、もみ10分程度放置した後、5kPa、30℃以下で迅速乾燥した結果、表4に示すようにインジカンがかなりの濃度で残存し、処理藍葉を水に懸濁し、毛束を処理した。若干薄いが染毛できた。ブランチング葉(酵素失活)に比べていずれもインジカン濃度は1/2〜1/3程度残存した。 Before microwave drying under reduced pressure, it was immersed in various aqueous solutions for the purpose of dulling the function of the enzyme, and after standing for about 10 minutes, it was rapidly dried at 5 kPa and 30 ° C. or less, as shown in Table 4. The indican remained at a significant concentration, and the treated mulberry leaves were suspended in water to treat the hair bundle. It was slightly thin, but I could dye. The indican concentration remained about 1/2 to 1/3 as compared with blanched leaves (enzyme inactivation).
ブランチング藍葉粉末20gに水250mlを加え、80℃、30分間加熱抽出した後、8,000rpm,20分間遠心分離することにより、インジカン溶液を作成した。酵素溶液は熟成藍葉粉末4gに水100mlを加え、室温で30分間撹拌した後、8,000rpm,20分間遠心分離することにより作成した。遠心分離後、上清を1μmのメンブレンフィルターで上記液体を濾過し、両者を混合した。タンパク質として小林ツエイン(小林香料(株))10gを混合溶液に添加し、室温で半日撹拌した。生成物は濾過し、室温で乾燥した。
得られた生成物は濃い藍色で、藍の色素がタンパク質に結合していると推測された。
An indican solution was prepared by adding 250 ml of water to 20 g of blanched mulberry powder, extracting by heating at 80 ° C. for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. The enzyme solution was prepared by adding 100 ml of water to 4 g of mature mulberry powder, stirring at room temperature for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. After centrifugation, the supernatant was filtered through a 1 μm membrane filter to mix the both. As a protein, 10 g of Kobayashi Twain (Kobayashi Fragrance Co., Ltd.) was added to the mixed solution and stirred at room temperature for half a day. The product was filtered and dried at room temperature.
The resulting product was dark amber and it was inferred that the silkworm pigment was bound to the protein.
ブランチング藍葉粉末20gに水250mlを加え、80℃、30分間加熱抽出した後、8,000rpm,20分間遠心分離することにより、インジカン溶液を作成した。酵素溶液は熟成藍葉粉末4gに水100mlを加え、室温で30分間撹拌した後、8,000rpm,20分間遠心分離することにより作成した。遠心分離後、上清を1μmのメンブレンフィルターで上記液体を濾過し、両者を混合した。糖としてβ-シクロデキストリン(和光純薬)10gを混合溶液に添加し、室温で半日撹拌した。生成物は濾過し、室温で乾燥した。
得られた生成物は濃い藍色で、藍の色素が糖に結合していると推測された。
An indican solution was prepared by adding 250 ml of water to 20 g of blanched mulberry powder, extracting by heating at 80 ° C. for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. The enzyme solution was prepared by adding 100 ml of water to 4 g of mature mulberry powder, stirring at room temperature for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. After centrifugation, the supernatant was filtered through a 1 μm membrane filter to mix the both. 10 g of β-cyclodextrin (Wako Pure Chemical Industries, Ltd.) as a sugar was added to the mixed solution and stirred at room temperature for half a day. The product was filtered and dried at room temperature.
The resulting product was dark amber and it was inferred that the amber pigment was attached to the sugar.
ブランチング藍葉粉末2gに水50mlを加え、80℃、30分間加熱抽出した後、8,000rpm,20分間遠心分離することにより、インジカン溶液を作成した。酵素溶液は熟成藍葉粉末0.4gに水10mlを加え、室温で30分間撹拌した後、8,000rpm,20分間遠心分離することにより作成した。遠心分離後、上清を1μmのメンブレンフィルターで上記液体を濾過し、両者を混合した。水溶性の糖としてグルコース(和光純薬)1gを混合溶液に添加し、室温で半日撹拌した後、静置した。凝集物は濾過し、室温で乾燥した。 An indican solution was prepared by adding 50 ml of water to 2 g of blanched mulberry powder, heating at 80 ° C. for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. The enzyme solution was prepared by adding 10 ml of water to 0.4 g of mature mulberry powder, stirring at room temperature for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. After centrifugation, the supernatant was filtered through a 1 μm membrane filter to mix the both. 1 g of glucose (Wako Pure Chemical Industries, Ltd.) as a water-soluble sugar was added to the mixed solution, stirred for half a day at room temperature, and allowed to stand. The aggregates were filtered and dried at room temperature.
ブランチング藍葉粉末20gに水250mlを加え、80℃、30分間加熱抽出した後、8,000rpm,20分間遠心分離することにより、インジカン溶液を作成した。酵素溶液は熟成藍葉粉末4gに水100mlを加え、室温で30分間撹拌した後、8,000rpm,20分間遠心分離することにより作成した。遠心分離後、上清を1μmのメンブレンフィルターで上記液体を濾過し、両者を混合した。タンパク質として小林ツエイン(小林香料(株))10gおよびグルコース10gを混合溶液に添加し、室温で半日撹拌した。生成物は濾過し、室温で乾燥した。得られた生成物は濃い藍色で、藍の色素がタンパク質に結合していると推測された。 An indican solution was prepared by adding 250 ml of water to 20 g of blanched mulberry powder, extracting by heating at 80 ° C. for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. The enzyme solution was prepared by adding 100 ml of water to 4 g of mature mulberry powder, stirring at room temperature for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. After centrifugation, the supernatant was filtered through a 1 μm membrane filter to mix the both. As a protein, 10 g of Kobayashi Twain (Kobayashi Fragrance Co., Ltd.) and 10 g of glucose were added to the mixed solution and stirred at room temperature for half a day. The product was filtered and dried at room temperature. The resulting product was dark amber and it was inferred that the silkworm pigment was bound to the protein.
水溶性の糖を添加することにより、インジゴがタンパク質表面で反応するだけでなく、凝集したより多くの有効成分がタンパク質(または糖)表面に沈着すると推測される。 By adding a water-soluble sugar, it is inferred not only that the indigo reacts on the protein surface but also that the aggregated more active ingredient is deposited on the protein (or sugar) surface.
ブランチング藍葉粉末20gに水250mlを加え、80℃、30分間加熱抽出した後、8,000rpm,20分間遠心分離することにより、インジカン溶液を作成した。酵素溶液は熟成藍葉粉末4gに水100mlを加え、室温で30分間撹拌した後、8,000rpm,20分間遠心分離することにより作成した。遠心分離後、上清を1μmのメンブレンフィルターで上記液体を濾過し、両者を混合した。タンパク質として上述の小林ツエイン(小林香料(株))10g、カゼイン10gまたはグルテン10gを混合溶液に添加し、室温で半日撹拌した。生成物は濾過し、室温で乾燥した。得られた生成物はいずれも濃い藍色で、藍の色素がタンパク質に結合していると推測された。
また、添加するタンパク質を変えることにより、タンパク質に吸着する藍成分の割合が変わることが確認できた。その分析結果を表5に示す。
An indican solution was prepared by adding 250 ml of water to 20 g of blanched mulberry powder, extracting by heating at 80 ° C. for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. The enzyme solution was prepared by adding 100 ml of water to 4 g of mature mulberry powder, stirring at room temperature for 30 minutes, and centrifuging at 8,000 rpm for 20 minutes. After centrifugation, the supernatant was filtered through a 1 μm membrane filter to mix the both. As a protein, 10 g of the above-mentioned Kobayashi Twain (Kobayashi Fragrance Co., Ltd.), 10 g of casein or 10 g of gluten were added to the mixed solution and stirred at room temperature for half a day. The product was filtered and dried at room temperature. The resulting products were all deep amber, and it was inferred that the silkworm pigment was bound to the protein.
In addition, it has been confirmed that changing the protein to be added changes the ratio of the soot component adsorbed to the protein. The analysis results are shown in Table 5.
本発明は、藍葉を低温マイクロ波熟成乾燥することにより、高機能性乾燥藍葉およびその粉末を製造でき、藍葉粉末を多くの有益な用途に用いることができるという付加価値を与えるものである。 The present invention provides the added value that high-performance dried mulberry leaves and their powders can be produced by low-temperature microwave ripening and drying mulberry leaves, and mulberry leaf powder can be used for many useful applications.
生藍葉にマイクロ波照射することで、藍葉中の酵素を活性化するとともに、酵素反応を促進・熟成して藍葉を熟成させることのできるマイクロ波熟成乾燥法を完成させることができた。この方法によれば、熟成乾燥が短時間で行え、しかも、インジカン分解酵素の活性が高められるだけでなく、タデ藍の主要な生理活性物質であり、抗菌活性、抗アレルギー活性、抗腫瘍活性を有するトリプタントリン、イサチンが1.5〜66倍以上の高濃度で含有することが確認された。本発明は、そのまま食することもできる機能性食品、化粧品、石鹸および医薬品としての用途にも用いられる高機能性乾燥藍葉粉末を提供し、さらに、藍葉中の酵素を失活させた乾燥藍葉粉末と混合した組成物は、染毛剤、染色剤としてだけでなく、沈殿藍用または藍顔料としてそれを添加した石鹸、クリーム等の化粧品は、アトピー性皮膚炎に効くことが期待され、また、青色に着色され、かつ生薬としての機能を有する機能性食品も製造できる。 By irradiating the raw mulberry leaves with microwaves, it was possible to complete the microwave ripening drying method which can activate the enzymes in the mulberry leaves and accelerate and age the enzyme reaction to ripen the mulberry leaves. According to this method, ripening and drying can be carried out in a short time, and not only the activity of indican degradation enzyme can be enhanced, but it is also a main physiologically active substance of Tade sputum, and has antibacterial, antiallergic and antitumor activities. It was confirmed that the tryptanthrin and isatin contained at a high concentration of 1.5 to 66 times or more. The present invention provides a highly functional dry mulberry leaf powder that can be used as it is for functional foods, cosmetics, soaps and pharmaceuticals, and further, it is a dry mulberry leaf powder in which enzymes in mulberry leaves are inactivated. The composition mixed with it is expected to be effective against atopic dermatitis as well as a hair dye and a staining agent, as well as cosmetics such as soaps and creams to which it is added as a precipitation glaze or a haze pigment. Functional foods which are colored in blue and have a function as a herbal medicine can also be produced.
また、熟成乾燥藍葉をアルコールなどで抽出すると、高機能成分を多く含んだ藍エキスが得られ、多方面に利用可能となる。
さらに、高トリプタントリン含量により、沈殿藍で染色した布は、アトピー性皮膚炎に効能のある布となり、また、染毛時には頭皮を保護するという効果も生じる。トリプタントリン含有量が高い乾燥藍葉を沈殿藍用として用いると、それを添加した石鹸、クリーム等の化粧品は、アトピー性皮膚炎に効き目があるので効能が高まる。
また、イサチン含量も高いため、パーキンソン病等に効果のある神経活性物質として用いられる可能性もある。
Further, when the matured dried mulberry leaves are extracted with alcohol or the like, a mulberry extract containing a large amount of high-performance components can be obtained and can be used in various fields.
Furthermore, due to the high triptanthrin content, the cloth stained with a precipitate becomes an effective cloth for atopic dermatitis, and also produces an effect of protecting the scalp when dyeing hair. When dry mulberry leaves having a high content of triptanthrin are used as a precipitate for chewing, cosmetics such as soaps and creams to which it is added have an effect on atopic dermatitis and thus the efficacy is enhanced.
In addition, since its isatin content is also high, it may be used as a neuroactive substance effective for Parkinson's disease and the like.
Claims (17)
加熱釜に接続される導波管と、
被照射物の温度を測定する温度センサと、
マイクロ波発振器と、
温度センサからの信号に基づきマイクロ波発振器を制御する制御プログラムを格納した記憶装置を備える制御装置とを備え、
前記制御プログラムが、請求項1ないし7のいずれかに記載の生藍葉のマイクロ波乾燥あるいは熟成乾燥方法を実行するための制御を行うことを特徴とするマイクロ波照射装置。 A heating pot in which the object to be irradiated is stored;
A waveguide connected to the heating kettle,
A temperature sensor that measures the temperature of the object to be irradiated;
Microwave oscillator,
A controller comprising a storage device storing a control program for controlling the microwave oscillator based on a signal from the temperature sensor;
A microwave irradiation apparatus characterized in that the control program performs control for executing the microwave drying or ripening drying method of ginger leaf according to any one of claims 1 to 7.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019157063A (en) * | 2018-03-16 | 2019-09-19 | 国立大学法人徳島大学 | Indigo leaves processed product-containing coloring agent |
CN112898800B (en) * | 2021-01-18 | 2022-09-16 | 山东云卿生物科技有限公司 | Method for extracting indigo |
KR20230077859A (en) * | 2021-11-26 | 2023-06-02 | 선문대학교 산학협력단 | Senior-friendly food comprising Perilla frutescens |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03274379A (en) * | 1990-03-26 | 1991-12-05 | Micro Denshi Kk | Normal pressure and low temperature micro wave drying |
JP2001327857A (en) * | 2000-05-22 | 2001-11-27 | Hitachi Ltd | Microwave drying equipment |
JP2003305425A (en) * | 2002-04-11 | 2003-10-28 | Mk Seiko Co Ltd | Garbage processing equipment |
JP2009149596A (en) * | 2007-11-29 | 2009-07-09 | Aiiro Kobo:Kk | A novel rapid extraction method of useful components in indigo leaves |
JP2013113448A (en) * | 2011-11-25 | 2013-06-10 | Seiko Engineering Kk | Microwave vacuum dryer, and drying method using the same |
WO2014104301A1 (en) * | 2012-12-28 | 2014-07-03 | 有限会社藍色工房 | Hair dye comprising dried indigo leaves and hair dyeing method using same |
-
2018
- 2018-08-30 JP JP2018161295A patent/JP7339714B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03274379A (en) * | 1990-03-26 | 1991-12-05 | Micro Denshi Kk | Normal pressure and low temperature micro wave drying |
JP2001327857A (en) * | 2000-05-22 | 2001-11-27 | Hitachi Ltd | Microwave drying equipment |
JP2003305425A (en) * | 2002-04-11 | 2003-10-28 | Mk Seiko Co Ltd | Garbage processing equipment |
JP2009149596A (en) * | 2007-11-29 | 2009-07-09 | Aiiro Kobo:Kk | A novel rapid extraction method of useful components in indigo leaves |
JP2013113448A (en) * | 2011-11-25 | 2013-06-10 | Seiko Engineering Kk | Microwave vacuum dryer, and drying method using the same |
WO2014104301A1 (en) * | 2012-12-28 | 2014-07-03 | 有限会社藍色工房 | Hair dye comprising dried indigo leaves and hair dyeing method using same |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2019157063A (en) * | 2018-03-16 | 2019-09-19 | 国立大学法人徳島大学 | Indigo leaves processed product-containing coloring agent |
JP7076058B2 (en) | 2018-03-16 | 2022-05-27 | 国立大学法人徳島大学 | Colorants containing processed indigo leaves |
CN112898800B (en) * | 2021-01-18 | 2022-09-16 | 山东云卿生物科技有限公司 | Method for extracting indigo |
KR20230077859A (en) * | 2021-11-26 | 2023-06-02 | 선문대학교 산학협력단 | Senior-friendly food comprising Perilla frutescens |
KR102644939B1 (en) * | 2021-11-26 | 2024-03-07 | 선문대학교 산학협력단 | Senior-friendly food comprising Perilla frutescens |
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