JP2530439B2 - Bath agent - Google Patents

Bath agent

Info

Publication number
JP2530439B2
JP2530439B2 JP61259461A JP25946186A JP2530439B2 JP 2530439 B2 JP2530439 B2 JP 2530439B2 JP 61259461 A JP61259461 A JP 61259461A JP 25946186 A JP25946186 A JP 25946186A JP 2530439 B2 JP2530439 B2 JP 2530439B2
Authority
JP
Japan
Prior art keywords
adsorbent
glucose
sugar
bath agent
powder
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.)
Expired - Lifetime
Application number
JP61259461A
Other languages
Japanese (ja)
Other versions
JPS63112511A (en
Inventor
暁美 門田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
OOSAKA YAKUHIN KENKYUSHO KK
Original Assignee
OOSAKA YAKUHIN KENKYUSHO KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by OOSAKA YAKUHIN KENKYUSHO KK filed Critical OOSAKA YAKUHIN KENKYUSHO KK
Priority to JP61259461A priority Critical patent/JP2530439B2/en
Publication of JPS63112511A publication Critical patent/JPS63112511A/en
Application granted granted Critical
Publication of JP2530439B2 publication Critical patent/JP2530439B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/96Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/97Cosmetics 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
    • A61K8/9783Angiosperms [Magnoliophyta]
    • A61K8/9794Liliopsida [monocotyledons]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Botany (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は浴用剤に係り、その目的は、浴用剤中に含
まれる染料、香料により生起されるアレルギー性皮膚炎
を防止することができ、しかも体温保温効果が高く、体
臭除去効果や皮膚の湿潤効果が高い浴用剤を提供するこ
とにある。
TECHNICAL FIELD The present invention relates to a bath agent, and an object thereof is to prevent allergic dermatitis caused by dyes and fragrances contained in the bath agent, Moreover, it is to provide a bath preparation having a high body temperature retention effect, a high body odor removal effect, and a high skin wetting effect.

(従来技術及びその欠点) 従来、浴用剤の配合は香料としてゲラニオール等を染
料としてウラニコン等をそれぞれ含んで構成されてい
る。
(Prior Art and Its Deficiencies) Conventionally, the composition of the bath agent is configured to include geraniol as a fragrance and uranicon as a dye.

このような浴用剤に配合される香料、染料のうちの多
くの物資はアレルゲンとして作用するものが多く、入浴
剤を添加した浴槽に入った入浴者の皮膚にアレルギー性
皮膚炎を生起させ易く、湿疹、皮膚炎症等を持つ人々は
使用できないという欠点があった。
Many of the fragrances and dyes mixed in such bath agents often act as allergens, and it is easy to cause allergic dermatitis on the skin of a bather who entered a bathtub containing a bath agent, It has the drawback that people with eczema, skin inflammation, etc. cannot use it.

又、従来の浴用剤は単に入浴時に湯水の色や香りを楽
しむだけのものが多く、入浴者の皮膚や健康増大や体臭
を除去する具体的な効果を発揮するものは全く存在しな
かった。
In addition, many conventional bath agents simply enjoy the color and scent of hot water when taking a bath, and none of them have a concrete effect of removing the skin and health of bathers and removing body odor.

(発明の経過) そこで、この発明者らは上記欠点を悉く解消するため
に鋭意研究したところ、染料、香料のアレルゲンとして
の機作を驚異的に抑制できしかも皮膚の健康の増大に効
果をもつ浴用剤を見いだした。即ち、粗糖、糖蜜等非精
製糖の水溶液を非極性の吸着剤に接触させて該吸着剤に
吸着される成分を必須成分とする浴用剤は浴用剤中の染
料、香料によって生起するアレルギー性皮膚炎の防止や
悪化抑制に大きな効果があるとともに体温上昇の保温効
果に優れしかも皮膚をしっとりとさせかつ体臭を除去で
きる効果をもつことを見いだし、この発明に至った。
(Progress of the invention) Therefore, the inventors of the present invention have conducted diligent research in order to eliminate the above-mentioned drawbacks. As a result, the mechanism of dyes and fragrances as an allergen can be surprisingly suppressed, and the effect of increasing skin health can be obtained. I found a bath agent. That is, a bath agent having an essential component that is adsorbed to a non-polar adsorbent by contacting an aqueous solution of unpurified sugar such as crude sugar and molasses with an adsorbent that is an allergic skin caused by a dye or fragrance in the bath agent The inventors have found that the present invention has a great effect on prevention of flames and suppression of deterioration, and also has an excellent effect of retaining body temperature, and has the effect of moisturizing the skin and removing body odor.

従来、粗糖、糖蜜等の非精製糖は脱色後、精製糖とし
て食用に供されるが、精製時に得られる吸着剤に吸着さ
れる成分は不用物として廃棄されるのみで、これを入浴
剤に使用すればアレルギーの予防や体臭除去効果や保温
効果があること等は一切知られていなかった。
Conventionally, unpurified sugar such as crude sugar and molasses is decolorized and then used as edible food as purified sugar.However, the components adsorbed by the adsorbent obtained during purification are simply discarded as unnecessary substances and used as bath salts. It was not known at all that it has the effects of preventing allergies, removing body odor, and retaining heat when used.

しかしこの発明者らは浴用剤の研究を深める過程で、
粗糖、糖蜜等非精製糖の水溶液を非極性の吸着剤に接触
させて該吸着剤に吸着される成分を必須成分として浴用
剤を調製すると従来の浴用剤の欠点を悉く解消できるこ
とを見いだしこの発明に到達した。
However, in the process of deepening the research on bath agents, the present inventors
It has been found that the drawbacks of conventional bath agents can be eliminated by preparing a bath agent by contacting an aqueous solution of unpurified sugar such as crude sugar and molasses with a non-polar adsorbent and using the components adsorbed by the adsorbent as essential components. Reached

(解決手段) 即ち、この発明は粗糖、糖蜜等非精製糖の水溶液を非
極性の吸着剤に接触させて該吸着剤に吸着される成分を
必須成分とする浴用剤に係るものである。
(Solution) That is, the present invention relates to a bath agent that contains an aqueous solution of unpurified sugar such as crude sugar and molasses in contact with a non-polar adsorbent, and the component adsorbed by the adsorbent is an essential component.

(発明の構成) この発明において使用する粗糖、糖蜜等非精製糖の水
溶液を非極性の吸着剤に接触させて該吸着剤に吸着され
る成分とは次の方法で得られるものを云う。
(Structure of the Invention) The component adsorbed to the adsorbent by bringing the aqueous solution of the unpurified sugar such as crude sugar and molasses into contact with the nonpolar adsorbent used in the present invention means the component obtained by the following method.

まず粗糖(いわゆる蔗糖の末精製品)、或いは糖蜜等
の非精製糖を通常の方法により砂糖黍または甜菜から準
備調製する。次いでこの粗糖等の非精製糖を適当量の水
に溶解しこれを吸着剤に接触させた後、吸着剤を水洗し
て糖分を更に充分除去し、その後吸着した成分を溶剤で
吸着剤から溶離する。通常、この溶離操作は吸着剤を充
填したカラムクロマト法によりおこなう。
First, crude sugar (so-called sucrose unrefined product) or unpurified sugar such as molasses is prepared and prepared from sugar cane or sugar beet by a conventional method. Next, this crude sugar or other unpurified sugar is dissolved in an appropriate amount of water, and this is contacted with the adsorbent, and then the adsorbent is washed with water to further remove sugar, and then the adsorbed component is eluted from the adsorbent with a solvent. To do. Usually, this elution operation is performed by a column chromatography method packed with an adsorbent.

この発明に使用する吸着剤としては非極性のポリスチ
レン系樹脂吸着例えばアンバーライトXAD−1、アンバ
ーライトXAD−2(ローム,アンド,ハース社製)及び
セルバクロムYAD−2(セルバ社製)が好適である。
尚。収率の点からはセルバクロムYAD−2が最も好まし
い。
As the adsorbent used in the present invention, nonpolar polystyrene-based resin adsorption such as Amberlite XAD-1, Amberlite XAD-2 (made by Rohm, And, Haas) and Selvachrome YAD-2 (made by Selva) are suitable. is there.
still. From the viewpoint of yield, cervachrome YAD-2 is most preferable.

この段階で得た吸着剤からの溶離物もこの発明におい
ては浴用剤として使用できる。即ち流出液を減圧下で濃
縮し、流エキス、軟エキス、乾燥エキスとして用いても
よい。
The eluate from the adsorbent obtained at this stage can also be used as a bath agent in the present invention. That is, the effluent may be concentrated under reduced pressure and used as a flow extract, soft extract, or dry extract.

尚、吸着剤の使用量は被吸着成分の30〜300倍(重
量)好ましくは50〜200倍が適当である。また、吸着し
た成分を溶離させるにあたっては、溶離前に洗液の甘味
が全くなくなるまで充分に糖分を水洗除去して洗浄流出
させると良い。
The adsorbent is used in an amount of 30 to 300 times (by weight), preferably 50 to 200 times, the amount of the adsorbed component. In addition, when eluting the adsorbed components, it is advisable to wash and wash out the sugars sufficiently before the elution until the washing liquid has no sweetness.

色素成分の溶離は濃度20%以上の低級アルコール例え
ばメタノール又はエタノールで行うのが好適である。実
際にはまず20〜30%の低濃度低級アルコールで溶離を行
い流下液の着色が殆ど認められなくなった後95〜99%程
度の高濃度低級アルコールでさらに溶離させるのが好ま
しい。高濃度低級アルコールのみで溶離を行うと収率が
低下するので好ましくない。
The elution of the dye component is preferably performed with a lower alcohol having a concentration of 20% or more, such as methanol or ethanol. In practice, it is preferable to first elute with a low-concentration lower alcohol of 20 to 30%, and after the coloring of the falling liquid is hardly observed, further elute with a high-concentration lower alcohol of about 95 to 99%. Elution with only a high-concentration lower alcohol is not preferable because the yield decreases.

このようにして得た溶離液を蒸発乾固した後、シリカ
ゲルカラムで精製分別すれば、白色のフェニルグルコー
ス化合物の粉末が得られる。この発明ではこのフェニル
グルコース化合物も浴用剤として利用する。このフェニ
ルグルコース化合物は粗糖、糖蜜等非精製糖の水溶液を
非極性の吸着剤に接触させて該吸着剤に吸着される成分
に含まれる特定オリゴ糖である。
The eluent thus obtained is evaporated to dryness, and then purified and fractionated by a silica gel column to obtain a white phenylglucose compound powder. In the present invention, this phenyl glucose compound is also used as a bath agent. The phenylglucose compound is a specific oligosaccharide contained in a component adsorbed to the adsorbent by contacting an aqueous solution of unpurified sugar such as crude sugar or molasses with the nonpolar adsorbent.

このようにして得た特定オリゴ糖の内フェニルグルコ
ース類は重量比で40%以上含まれ特に3,4−ジメトキシ
フェニル−O−D−グルコースは特定オリゴ糖の内20%
程度以上、又、または3,4,6−トリメトキシ−O−D−
フェニルグルコースは約10%程度含有する。
The specific oligosaccharides thus obtained contained 40% or more by weight of phenylglucose, and particularly 3,4-dimethoxyphenyl-OD-glucose contained 20% of the specific oligosaccharides.
Or more, or 3,4,6-trimethoxy-OD-
Contains about 10% phenyl glucose.

この吸着剤に吸着される成分の内作用成分は主として
特定オリゴ糖であるが、その内フェニルグルコース類が
40%以上を占め、又フェニルグルコース類中3,4−ジメ
トキシフェニル−O−D−グルコース及び3,4,6−トリ
メトキシ−O−D−フェニルグルコースは15%以上を占
める。
The internal acting components of the components adsorbed by this adsorbent are mainly specific oligosaccharides, of which phenylglucose is
It accounts for 40% or more, and 3,4-dimethoxyphenyl-OD-glucose and 3,4,6-trimethoxy-OD-phenylglucose account for 15% or more in phenylglucose.

この実験的知得はGLC,TLC,NMR,IR,UV等の常法の定
性,定量分析によって行われた。
This experimental knowledge was obtained by qualitative and quantitative analysis by conventional methods such as GLC, TLC, NMR, IR, and UV.

この発明においては、フェニルグルコース化合物は有
機合成方法によって、フェニル基とグルコース基を化学
的にエーテル結合されたものであってもよく、その合成
方法としては特に限定されるものではない。
In the present invention, the phenyl glucose compound may be one in which a phenyl group and a glucose group are chemically ether-bonded by an organic synthesis method, and the synthesis method is not particularly limited.

官能基としてメトキシル基がC3及びC4及び要約すれば
C6の位置に置換された3,4−メトキシフェニル基又は3,
4,6−メトキシフェニル基とグルコース基をエーテル結
合させる合成方法で合成されたフェニルグルコース化合
物でも良い。
If the methoxyl group as a functional group is C3 and C4
A 3,4-methoxyphenyl group substituted at the C6 position or 3,
A phenylglucose compound synthesized by a synthetic method in which a 4,6-methoxyphenyl group and a glucose group are ether-bonded may be used.

この発明で使用する特定オリゴ糖であるフェニルグル
コース化合物は次式で表される。
The phenylglucose compound which is the specific oligosaccharide used in the present invention is represented by the following formula.

3,4−ジメトキシフェニル−O−D−グルコースを
(式I)で、3,4,6−トリメトキシフェニル−O−D−
グルコース(式II)で表す。
3,4-dimethoxyphenyl-O-D-glucose was converted to (formula I) with 3,4,6-trimethoxyphenyl-OD-
It is represented by glucose (formula II).

この発明ではこのフェニルグルコース化合物を合成
法,天然物抽出法の何れの方法で得ても良いし、又この
両者を混合しても良い。また、必要に応じて他の成分を
添加してもよい。
In the present invention, the phenylglucose compound may be obtained by either synthetic method or natural product extraction method, or both may be mixed. Moreover, you may add another component as needed.

この他の成分としては、ヘチマ、パパイヤ酵素、甘
草、カンキツ類、アマチャヅルを挙げることができる。
Examples of other components include loofah, papaya enzyme, licorice, citrus and army cucumber.

この発明で使用するヘチマとは従来公知のヘチマ例え
ば、だるま種、ナガイトウリ種、トカドヘチマ種等全て
をいい、この発明で好適に使用できるこのヘチマ(Luff
a cylindrica)の部位としては全草、果実、若い果実、
種子、つる、ヘチマ水の全てであり特に果実(種子も含
む)が最も望ましい。
The loofah used in the present invention refers to all of the conventionally known loofahs, for example, Daruma seeds, Nagaitouri seeds, tocad loofah seeds, and the like, which are preferably used in the present invention (Luff
a cylindrica) parts of whole grass, fruits, young fruits,
Seeds, vines, and loofah water are all preferred, and fruits (including seeds) are most desirable.

この様なヘチマを浴用剤に配合するには、乾燥粉末、
抽出エキス液、抽出エキス粉末、搾汁等の形態とすれば
よい。
To mix such loofah with a bath agent, dry powder,
It may be in the form of extract liquid, extract powder, squeezed juice or the like.

抽出エキスとするには、低級脂肪族アルコール、エー
テル類等の炭素数1〜9の脂肪性有機溶媒が有効に使用
できる。
For the extract, an aliphatic organic solvent having 1 to 9 carbon atoms such as lower aliphatic alcohol and ethers can be effectively used.

このような抽出エキス液から抽出エキス粉末を得るに
は、凍結乾燥、減圧乾燥、噴霧乾燥等の任意乾燥手段を
採用すればよい。
In order to obtain the extract powder from such extract liquid, any drying means such as freeze-drying, reduced pressure drying, and spray drying may be adopted.

この発明で使用する甘草とは、学名をGLYCYRRH−IZAE
RADIXといい、マメ科(Leguminosae)のナンキンカン
ゾウ(西北甘草)Glycyrrhiza glabra L.var.glan duli
fera Reg.et Herd(=G.glandu−lifera Waldstein et
Kitaibel)及びウラルカンゾウ(東北甘草)Glycyrrhiz
a uralensis Fisch.et DC.の根及びストロンを乾燥した
ものが好ましく用いられる。
Licorice used in the present invention is scientifically named GLYCYRRH-IZAE.
It is called RADIX, a legume (Leguminosae) peanut licorice (northwest licorice) Glycyrrhiza glabra L.var.glan duli
fera Reg.et Herd (= G.glandu-lifera Waldstein et
Kitaibel) and Uralkanzo (Tohoku licorice) Glycyrrhiz
The dried roots and stron of a uralensis Fisch.et DC. are preferably used.

この発明において、上記甘草を浴用剤中に配合するに
は、甘草の粉末又は熱水抽出エキスの形態とすればよ
い。
In the present invention, the licorice may be incorporated into the bath agent in the form of licorice powder or hot water extract.

この発明で使用するアマチャヅル(Gynostemmap−ent
aphyllum Makino)としては、アマチャヅルの全部位地
上部又は地下部、或いは種子が好適に使用できる。
Armored crane (Gynostemmap-ent) used in this invention
As aphyllum Makino), all parts above ground or below ground, or seeds of army vine can be preferably used.

これらを用いてこの発明の配合成分とするには、まず
これらを生のままで粉砕し、圧搾して搾汁を得る。この
搾汁はアマチャヅルを混合して行ってもよく、或いは別
途にそれぞれ処理してもよい。この搾汁は希釈して使用
する、或いは凍結乾燥、噴霧乾燥して粉末状で使用する
ことができる。或いは、これらの原材料を風乾、熱風乾
燥して、乾燥粉末としてもよい。
In order to use them as the compounding ingredients of the present invention, they are first ground as they are and pressed to obtain juice. This squeezing may be carried out by mixing armchair or may be separately processed. This squeezed juice can be used by diluting it, or can be used in powder form by freeze-drying or spray-drying. Alternatively, these raw materials may be air dried or hot air dried to obtain a dry powder.

更に、低級含水アルコール等の溶媒で抽出し、この抽
出液を濃縮する或いは希釈する、更には噴霧乾燥、凍結
乾燥等の手法でこの抽出液を粉末にして使用してもよ
い。
Furthermore, the extract may be used as a powder by extraction with a solvent such as a lower hydrous alcohol and concentrating or diluting the extract, and further by spray drying, freeze drying or the like.

この発明で配合成分として使用できるカンキツ類とし
ては、キシューミカン(Citrus Kinokuni Hort.ex Tana
ka),ウンシューミカン(Citrusunshu Marc.),クネ
ンボ(Citrus nobilis Lour),ユズ(Citrus junos Si
eb.ex Tanaka),イヨミカン(Citrus iyo Hort.ex Tan
aka),ネーブル(Cit−rus sinensis Osheck var bras
iliensis Tanaka),ダイダイ(Citrus aurantium L.F.
kabos Y.Tan−aka),等のカンキツ類が全て好適に使用
できる。
Citrus citrus (Citrus Kinokuni Hort.ex Tana) can be used as a citrus compound in the present invention.
ka), Unshu mikan (Citrusunshu Marc.), Kunebo (Citrus nobilis Lour), Yuzu (Citrus junos Si)
eb.ex Tanaka), Citrus iyo Hort.ex Tan
aka), Navel (Cit-rus sinensis Osheck var bras
iliensis Tanaka), Daidai (Citrus aurantium LF)
Kabos Y. Tan-aka), etc. can all be suitably used.

これらカンキツ類の外皮の乾燥物の粉末が、配合成分
としてはより望ましい。
The powder of the dried product of the outer skin of these citrus fruits is more desirable as a compounding ingredient.

以上のような、この発明に係る配合成分を使用してこ
の発明に係る浴用剤とするには、常法に準じて公知の増
量剤、香料、染料の添加剤を加え、任意の入浴剤形態に
調製すればよい。
As described above, in order to obtain the bath agent according to the present invention by using the compounding ingredients according to the present invention, a known extender, a fragrance, and an additive for a dye are added according to a conventional method, and any bathing agent form is added. It may be prepared.

この発明に係る浴用剤を調製するには、例えばラウリ
ル硫酸ナトリウム40g、ラウリルジメチルアミノ酢酸ベ
タイン20g、精製水35g、香料1g、染料適量に対して、白
色粉末を0.01〜1g好ましくは0.02g、フェニルグルコー
ス化合物であれば0.005g〜1g好ましくは0.01gを配合
し、パパイヤ酵素を配合する場合は1〜5g好ましくは2
g、ヘチマサポチンを配合する場合は抽出エキス粉末で
0.5〜5g好ましくは1g、甘草を配合する場合は天然乾燥
粉末で2〜8g好ましくは5g、アマチャヅルを配合する場
合は抽出エキス粉末で2〜4g好ましくは3g、ユズを配合
する場合はユズ皮の乾燥粉末で2〜6g好ましくは3gとす
る。
To prepare the bath agent according to the present invention, for example, sodium lauryl sulfate 40 g, lauryl dimethylamino acetic acid betaine 20 g, purified water 35 g, perfume 1 g, dye suitable amount, 0.01-1 g of white powder, preferably 0.02 g, phenyl If it is a glucose compound, 0.005 g to 1 g, preferably 0.01 g is blended, and if a papaya enzyme is blended, 1 to 5 g, preferably 2 g.
g, when blending luffa sapotin with extract powder
0.5 to 5 g, preferably 1 g, natural dry powder 2 to 8 g preferably 5 g when licorice is blended, extract extract powder 2 to 4 g preferably 3 g when armature is blended, and yuzu peel of yuzu is blended The amount of dry powder is 2 to 6 g, preferably 3 g.

(効果) 以上詳述した如く、この発明に係る浴用剤は、浴用剤
中に配合されるアレルゲン性の染料や香料のアレルゲン
としての機作を弱め、かつ体温保持特性に優れ皮膚の湿
潤効果や体臭除去効果をもつという効果を奏する。
(Effect) As described in detail above, the bath agent according to the present invention weakens the mechanism of the allergenic dye or fragrance contained in the bath agent as an allergen, and is excellent in body temperature retention property and has a moisturizing effect on the skin. It has the effect of removing body odor.

以下、この発明の実施例、並びに試験例を記載するこ
とにより、この発明の優れた効果をより一層明確なもの
とする。
Hereinafter, the excellent effects of the present invention will be further clarified by describing Examples and Test Examples of the present invention.

(実施例) 沖縄産黒砂糖5kgを水25に溶解し、ポリスチレン系
樹脂(セルバクロムXAD−2.300g)を水1に分散させ
て充填した内径8cmのカラムに注入し、20ml/分の速度で
流下させ黒砂糖の色素成分を吸着させる。
(Example) 5 kg of brown sugar from Okinawa was dissolved in 25 water, and polystyrene resin (Cervachrome XAD-2.300 g) was dispersed in 1 water and poured into a packed column having an inner diameter of 8 cm, followed by flowing at a rate of 20 ml / min. Then, the pigment component of brown sugar is adsorbed.

次に水を流下させ甘味の全くなくなるまで水洗して充
分に糖分を除く。
Next, water is poured down and washed with water until the sweetness is completely removed to remove sugar sufficiently.

流下液に甘味が全くなくなってから20%メタノールを
注入し、10ml/分の速度で流下させ吸着剤から色素を溶
離させる。
After the flow-through solution has no sweetness at all, 20% methanol is injected and the dye is eluted from the adsorbent at a flow rate of 10 ml / min.

流下液に着色が全くなくなるまで流下を続ける。 Continue to flow down until there is no color in the flow-through.

両流下溶離液を合し、60℃以下で減圧蒸発乾固し、褐
色残留物16gを得る。
Both eluents flowing down are combined and evaporated to dryness under reduced pressure below 60 ° C. to obtain 16 g of a brown residue.

このものを2の純エタノールに加熱して溶かし、冷
却後、析出した濁り物質を濾別し、60℃以下で減圧蒸発
乾固し、その残留物を60℃以下で乾燥して甘味の全くな
い白色粉末15gを得る。
This product was dissolved in 2 pure ethanol by heating, and after cooling, the precipitated turbid substance was filtered off and evaporated to dryness under reduced pressure at 60 ° C or lower, and the residue was dried at 60 ° C or lower to have no sweetness. 15 g of white powder are obtained.

以上説明したような操作によって得られた白色粉末
は、以下の薄層クロマトグラフィーのRF値及び赤外吸収
スペクトルの吸収値からフェニルグルコースが作用成分
であった。
In the white powder obtained by the above-described operation, phenylglucose was the active ingredient from the RF value and the absorption value of the infrared absorption spectrum of the following thin layer chromatography.

薄層クロマトグラフィー; 10mgを水1mlに溶解し下記条件により日本薬局法一般
試験法第26項薄層クロマトグラフ法により試験をすると
き、RF値役0.6に単一の紅色スポットを示す。
Thin-layer chromatography: When 10 mg is dissolved in 1 ml of water and tested by the Japanese Pharmacopoeia General Test Method Section 26 thin-layer chromatography under the following conditions, a single red-colored spot is shown at an RF value of 0.6.

試料添付量:10μ 担体:シリカゲル60F254(メルク社製 厚さ0.25mm) 展開溶媒:クロロホルム・メタノール・水(65:35:10)
下層 展開距離:10cm 検出:P−アニスアルデヒド試験噴霧後、105℃で5分間
加熱 このスポットは3,4−メトキシフェニルグルコース及
び3,4,6−メトキシフェニルグルコースの混合物と同一
スポットであった。
Amount of sample attached: 10μ Carrier: Silica gel 60F254 (Merck 0.25 mm thickness) Developing solvent: Chloroform / methanol / water (65:35:10)
Lower layer Development distance: 10 cm Detection: P-anisaldehyde After test spraying, heating at 105 ° C. for 5 minutes This spot was the same spot as the mixture of 3,4-methoxyphenyl glucose and 3,4,6-methoxyphenyl glucose.

赤外線吸収スペクトル; νmax(ヌジョール):3300、1590、1020及び720cm−1 この赤外線吸収スペクトルは、メトキシルで置換され
たフェニルグルコースであることを示す。
Infrared absorption spectrum; νmax (nujol): 3300, 1590, 1020 and 720 cm -1 This infrared absorption spectrum shows phenyl glucose substituted with methoxyl.

この物質の同定法は後記詳述する。 The method for identifying this substance will be described in detail later.

得られた褐色粉末を500ccメタノールに溶解し、クロ
ロホルム・メタノール・水混液の流下溶液を用いてシリ
カゲルカラムによりカラムクロマトグラフ精製し3,4−
メトキシフェニル−O−D−グルコース及び3,4,6−メ
トキシフェニル−O−D−グルコースに分別した。
The brown powder obtained was dissolved in 500 cc of methanol, and purified by column chromatography using a silica gel column using a flowing solution of a mixture of chloroform, methanol, and water.
It was fractionated into methoxyphenyl-OD-glucose and 3,4,6-methoxyphenyl-OD-glucose.

上記白色粉末と、3,4−メトキシフェニル−O−D−
グルコースと、3,4,6−メトキシフェニル−O−D−グ
ルコースとを用いて以下のような浴用剤を調製した。
The above white powder and 3,4-methoxyphenyl-OD-
The following bath preparation was prepared using glucose and 3,4,6-methoxyphenyl-OD-glucose.

(実施例1) ヘチマの果実を裁断してエタノールに浸漬し、ヘチマ
サポニンを抽出し、抽出液を減圧乾燥してヘチマ抽出エ
キス粉末とする。
(Example 1) A loofah fruit is cut and immersed in ethanol to extract loofah saponin, and the extract is dried under reduced pressure to obtain loofah extract powder.

このエキス粉末とパパイヤ酵素と白色粉末とを下記の
通りに配合して浴用剤を得る。
The extract powder, papaya enzyme and white powder are blended as described below to obtain a bath agent.

ラウリル硫酸ナトリウム 40.0 g ラウリルジメチルアミノ酢酸ベタイン 20.0 g 精製水 35.0 g ゲラニオール(香料) 1.0 g ウラニンコンク(染料) 適量 ヘチマ抽出エキス粉末 1.0 g パパイヤ酵素 2.0 g 白色粉末 0.05g (実施例2) 甘草を天然乾燥によって乾燥させた後、粉砕する。Sodium lauryl sulfate 40.0 g Betaine lauryldimethylaminoacetate 20.0 g Purified water 35.0 g Geraniol (fragrance) 1.0 g Uranine conc (dye) Appropriate amount Luffa extract extract powder 1.0 g Papaya enzyme 2.0 g White powder 0.05 g (Example 2) Natural licorice After drying by drying, it is ground.

上記甘草粉末と白色粉末を下記の通りに配合して浴用
剤を得た。
The above licorice powder and white powder were blended as described below to obtain a bath agent.

ラウリル硫酸ナトリウム 40.0 g ラウリルジメチルアミノ酢酸ベタイン 20.0 g 精製水 35.0 g ゲラニオール 1.0 g ウラニンコンク(染料) 適量 甘草粉末 5 g 白色粉末 0.02g (実施例3) アマチャヅルを裁断し、その裁断物を60℃の熱水中に
浸漬して、裁断中の熱水抽出エキスを熱水中に溶出せし
め、その後濾過し、濾液を得る。
Sodium lauryl sulphate 40.0 g Lauryl dimethylaminoacetic acid betaine 20.0 g Purified water 35.0 g Geraniol 1.0 g Uranine conc (dye) Appropriate amount Licorice powder 5 g White powder 0.02 g (Example 3) It is immersed in hot water to elute the hot water extraction extract being cut into hot water and then filtered to obtain a filtrate.

同濾液を濃縮した後、減圧乾燥させて熱水抽出エキス
粉末とする。
The filtrate is concentrated and then dried under reduced pressure to obtain hot water extract powder.

上記アマチャヅル粉末と3,4−メトキシフェニル−O
−D−グルコースを下記の通りに配合して浴用剤を得
た。
The above powdered armchair and 3,4-methoxyphenyl-O
-D-Glucose was blended as described below to obtain a bath agent.

ラウリル硫酸ナトリウム 40.0 g ラウリルジメチルアミノ酢酸ベタイン 20.0 g 精製水 35.0 g ゲラニオール(香料) 1.0 g ウラニンコンク(染料) 適量 アマチャヅル粉末 3.0 g 3,4−ジメトキシフェニル−O−D−グルコース 0.01g (実施例4) ユズ外皮を乾燥させた後、粉末化した。Sodium lauryl sulphate 40.0 g Lauryl dimethylamino acetic acid betaine 20.0 g Purified water 35.0 g Geraniol (fragrance) 1.0 g Uranine conc (dye) Appropriate amount of armchaise powder 3.0 g 3,4-dimethoxyphenyl-OD-glucose 0.01 g (Example 4) ) The yuzu hull was dried and then pulverized.

このユズ粉末と3,4,6−トリメトキシフェニル−O−
D−グルコースを下記の通りに配合して浴用剤を得た。
This Yuzu powder and 3,4,6-trimethoxyphenyl-O-
D-Glucose was blended as described below to obtain a bath preparation.

ラウリル硫酸ナトリウム 40.0 g ラウリルジメチルアミノ酢酸ベタイン 20.0 g 精製水 35.0 g ゲラニオール(香料) 1.0 g ウラニンコンク(染料) 適量 ユズ粉末 3.0 g 3,4,6−トリメトキシフェニル−O−D−グルコース0.0
1g (比較例1) 実施例1から白色粉末を除いたものを使用した。
Sodium lauryl sulfate 40.0 g Betaine lauryl dimethylaminoacetate 20.0 g Purified water 35.0 g Geraniol (fragrance) 1.0 g Uranine conc (dye) Appropriate amount Yuzu powder 3.0 g 3,4,6-Trimethoxyphenyl-OD-glucose 0.0
1 g (Comparative Example 1) The product obtained by removing the white powder from Example 1 was used.

(比較例2) 実施例2から白色粉末を除いたものを使用した。(Comparative Example 2) The product obtained by removing the white powder from Example 2 was used.

(比較例3) 実施例3から3,4−ジメトキシフェニル−O−D−グ
ルコースを除いたものを使用した。
(Comparative Example 3) The one obtained by removing 3,4-dimethoxyphenyl-OD-glucose from Example 3 was used.

以上の浴用剤を比較的体臭のある冷え症の女性20人
(18〜45才)に3日間づつ計15日間試用した。
The above bath agents were tested on 20 females (18-45 years old) with chilling who had a relatively body odor for 3 days, 15 days in total.

尚、濃度は0.01wt%程度浴湯に溶かした。 The concentration was about 0.01 wt% dissolved in bath water.

結果を第1表及び第2表に示す。 The results are shown in Tables 1 and 2.

以上の結果から、この発明に係る浴用剤は驚異的なア
レルギー性皮膚炎の防止効果及び優れた保温効果更には
体臭消臭効果、皮膚湿潤効果があることがわかる。
From the above results, it can be seen that the bath preparation according to the present invention has a surprising effect of preventing allergic dermatitis, an excellent heat retaining effect, a body odor eliminating effect, and a skin moisturizing effect.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】粗糖、糖蜜等非精製糖の水溶液を非極性の
吸着剤に接触させて該吸着剤に吸着される成分を必須構
成とする浴用剤。
1. A bath agent comprising as an essential component a component which is adsorbed on a non-polar adsorbent by bringing an aqueous solution of unpurified sugar such as crude sugar and molasses into contact with the non-polar adsorbent.
【請求項2】請求項(1)に記載の粗糖、糖蜜等非精製
糖の水溶液を非極性の吸着剤に接触させて該吸着剤に吸
着される成分が3,4−ジメトキシフェニル−O−D−グ
ルコース及び/又は3,4,6−トリメトキシフェニル−O
−D−グルコースである請求項1に記載の浴用剤。
2. A component adsorbed to the adsorbent by contacting the aqueous solution of the unpurified sugar such as the crude sugar or molasses according to claim 1 with the nonpolar adsorbent is 3,4-dimethoxyphenyl-O-. D-glucose and / or 3,4,6-trimethoxyphenyl-O
The bath agent according to claim 1, which is -D-glucose.
JP61259461A 1986-10-30 1986-10-30 Bath agent Expired - Lifetime JP2530439B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61259461A JP2530439B2 (en) 1986-10-30 1986-10-30 Bath agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61259461A JP2530439B2 (en) 1986-10-30 1986-10-30 Bath agent

Publications (2)

Publication Number Publication Date
JPS63112511A JPS63112511A (en) 1988-05-17
JP2530439B2 true JP2530439B2 (en) 1996-09-04

Family

ID=17334389

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61259461A Expired - Lifetime JP2530439B2 (en) 1986-10-30 1986-10-30 Bath agent

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Country Link
JP (1) JP2530439B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012172049A (en) * 2011-02-21 2012-09-10 Masatsugu Yamashita Deodorizing detergent
JP2012219228A (en) * 2011-04-12 2012-11-12 Masatsugu Yamashita Water-soluble black pigment
CN115671017A (en) * 2018-04-27 2023-02-03 一丸自然美健有限公司 Liquid containing saccharide and distiller's grains

Also Published As

Publication number Publication date
JPS63112511A (en) 1988-05-17

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