JPS59204114A - Powdery makeup cosmetic - Google Patents

Powdery makeup cosmetic

Info

Publication number
JPS59204114A
JPS59204114A JP7991883A JP7991883A JPS59204114A JP S59204114 A JPS59204114 A JP S59204114A JP 7991883 A JP7991883 A JP 7991883A JP 7991883 A JP7991883 A JP 7991883A JP S59204114 A JPS59204114 A JP S59204114A
Authority
JP
Japan
Prior art keywords
skin
whitening
enzyme
powder
immobilized
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.)
Granted
Application number
JP7991883A
Other languages
Japanese (ja)
Other versions
JPH0458442B2 (en
Inventor
Kazuyoshi Morita
和良 森田
Kunio Mimura
邦雄 三村
Takashi Abe
隆 安部
Kyotaro Hasunuma
蓮沼 喬太郎
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.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP7991883A priority Critical patent/JPS59204114A/en
Publication of JPS59204114A publication Critical patent/JPS59204114A/en
Publication of JPH0458442B2 publication Critical patent/JPH0458442B2/ja
Granted legal-status Critical Current

Links

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
    • A61K8/64Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/66Enzymes
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/12Face or body powders for grooming, adorning or absorbing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/57Compounds covalently linked to a(n inert) carrier molecule, e.g. conjugates, pro-fragrances
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/74Biological properties of particular ingredients
    • A61K2800/75Anti-irritant

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

PURPOSE:To provide a powdery makeup cosmetic free from side effects and skin irritation, absorbable easily through the skin, and exhibiting extremely high skin- beautifying effect, by compounding a specific straight-chain dibasic acid mono- or diester as a skin-beautifying component, together with an immobilized enzyme. CONSTITUTION:The objective powdery makeup cosmetic can be prepared by using one or more compounds of formula (R1 and R2 are 1-8C straight-chain alkyl or akenyl; R2 may be H; n is integer of 1-13) as a skin-beautifying component together with an immobilized enzyme, preferably the powder of protease or amylase immobilized to a carrier composed of a polymeric substance. The amounts of the skin-beautifying component and the immobilized enzyme are 10- 25wt% and 0.5-10wt%, respectively, based on the whole cosmetic preparation, and the content of enzyme in the immobilized enzyme is 5-20wt%. The beautifying component is safe to the skin even at a high rate of compounding, and is free of skin irritation. The combined use of the component with the immobilized enzyme promotes the transcutaneous absorption, and develops high and long- acting skin-beautifying effect.

Description

【発明の詳細な説明】 本発明は新規な美白粉末化粧料に関し、詳しくは、人体
に好ましくない副作用や皮1* 11激がなく、固定化
酵素によって彼記の一般式で表わされるエステル(以F
直鎖u2塩基酸エステルさいう)の経vl吸収性を容易
にし、著しく優れた美白効果を発現しうる新規な美白粉
末化粧料である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel skin-whitening powder cosmetic, and more particularly, it has no undesirable side effects or skin irritation on the human body, and is made by immobilized enzymes to produce an ester (hereinafter referred to as F
This is a novel skin-whitening powder cosmetic that facilitates the trans-VL absorption of linear U2 basic acid esters and exhibits outstanding whitening effects.

色黒のp因は、過剰の日光光線特に紫外線の反膚照射に
よって、皮膚内のチロシンがチロシナーセ°の作用(活
性)により酸化され、ドー〆(−になり、さらにドーパ
−キノンを経て5,6−ジヒドロインドールになりこれ
が重合してメラニン(色素)を生成することにあるとさ
れている。
The cause of dark skin is that when the skin is irradiated with excessive sunlight, especially ultraviolet rays, tyrosine in the skin is oxidized by the action (activity) of tyrosinase°, becoming dopa-quinone (-), and then 5, It is believed that 6-dihydroindole is formed and this polymerizes to produce melanin (pigment).

日焼けしfcyLは、これらメラニン色票の増加した状
態にあるので、肌色の回復ICは既成のメラニンの淡色
漂白化やメラニン生成過桿でのチロシナーゼ活性の阻害
等が必要である。
Since tanned fcyL is in a state where these melanin color spots are increased, skin color restoration IC requires bleaching of existing melanin and inhibition of tyrosinase activity in melanin-producing rods.

従来より、ビタミンC1システイン、コロイド硫黄など
を配合した化粧料が囲発され賞月されているが、これら
は充分に満足し得る保存性、安定性および美白効果を有
するものとは言い難い。
Cosmetics containing vitamin C1, cysteine, colloidal sulfur, and the like have been developed and praised, but these cannot be said to have sufficiently satisfactory storage stability, stability, and whitening effect.

特開昭53−150443号公報には、色素過多症皮膚
病の治療を目的とした治療用組成物(実施例乙には活性
成分のアゼライン酸とビタミンCと角質溶解剤としての
クロロクレゾール、ヅリチル酸を、多量のラクリル硫酸
ナトリクム(強い皮膚φ1■激を有することは周知)を
含むクリーム基剤に配合したクリーム状組成物、実施例
9のfalにはアゼライン酸とビタミンCとアゼライン
酸ジメチルエステルを食塩水に溶解した腹腔内注射用組
成物、実施例9の(clにはドデカンジオスック酸(L
IO−デカメチレンジカルボン酸とビタミンcとドデカ
ンジオイック酸ジメチルエステルを食塩水に溶解したラ
ド注射用組成物〕および治療法が概説されている。
JP-A-53-150443 discloses a therapeutic composition for the treatment of hyperpigmented skin diseases (Example B contains active ingredients azelaic acid, vitamin C, and keratolytic agents chlorocresol and durityl). A cream composition in which an acid is blended into a cream base containing a large amount of sodium lacryl sulfate (known to have a strong skin φ1).Fal of Example 9 contains azelaic acid, vitamin C, and azelaic acid dimethyl ester. An intraperitoneal injection composition prepared by dissolving in saline, a composition for intraperitoneal injection of Example 9 (cl is dodecanediosuccinic acid (L)).
A RAD injectable composition containing IO-decamethylene dicarboxylic acid, vitamin c, and dodecanedioic acid dimethyl ester dissolved in saline] and treatment methods are outlined.

しかしながら、か\る治療用組成物は当該皮膚病の治療
が適用できたとしても、美白化粧料の如く肌に刺激を与
えることなく、挺康な皮膚を適度良好に美白化し、ある
いけシミ、ソバカス等を軽減する目的には適さない。何
故ならば、か\る皮膚病治療用lII成物酸物、健康な
(皮膚病ではないり皮膚に施用すると強い刺激を与え、
角質を溶解する等の他、チロシナーゼの活性を適度に阻
害できず、その結果実用的な美白効果が得られないから
である。
However, even if such therapeutic compositions can be applied to the treatment of the skin disease, they do not irritate the skin like whitening cosmetics do, whiten healthy skin to a moderate degree, and eliminate blemishes and blemishes. Not suitable for the purpose of reducing freckles etc. This is because some type II compound acids used to treat skin diseases can cause strong irritation when applied to healthy (not skin disease) skin.
This is because, in addition to dissolving stratum corneum, it cannot adequately inhibit tyrosinase activity, and as a result, no practical whitening effect can be obtained.

零発明者等d1か\る現状に鑑み、人体に好ましくない
副作用を有さす、かつ良好な美白効果を奏し得る美白化
粧料について、鋭意広範囲な系統的研究を行なった結果
、後記一般式で表わされるエステル(直鎖構造の2塩基
酸モノエステル又hジエステル)は、多量配合しても安
全で皮膚刺激がなく、その上固定化酵素と併用する場合
は、非常に容易かつ速やかをて皮膚内に吸収されて、存
在するチロシナーゼ活性を適度に阻害して顕著なメラニ
ン生成の抑制作用を示すと共に、優れた美白効果を発現
し、また当該化粧P1の製品を長期保存しても極めて安
定で、矢白能を永く保持し得ることを見出し、不発1月
を完成した。
In view of the current situation, the inventors have conducted extensive and systematic research on whitening cosmetics that have unfavorable side effects on the human body and have good whitening effects. The esters (linear dibasic acid monoesters or h-diesters) are safe and do not irritate the skin even when mixed in large amounts, and when used in combination with immobilized enzymes, they can be easily and quickly absorbed into the skin. It moderately inhibits the existing tyrosinase activity and exhibits a remarkable suppressive effect on melanin production, and also exhibits an excellent whitening effect, and is extremely stable even when the cosmetic P1 product is stored for a long time. He discovered that Yajiro Noh could be maintained for a long time, and completed the dud January.

すなわち、木兄il!FIは、美白剤成分(活性成分)
として、ド記一般式 %式% (上記式中で、R1け炭素数1〜8の直鎖状のアルキル
基またけアルケニル基、R8け水素原子またii炭素数
1〜8の直鎖状のアルキル基、あるいけアルケニル基で
あり、nは1〜13の整数である。) で表わされるエステルの少なくとも1つが固定化酵素と
共に配合されていることを特徴とする美白粉末化粧料で
ある。
In other words, Ki-nii il! FI is a whitening agent ingredient (active ingredient)
(In the above formula, R1 is a linear alkyl group having 1 to 8 carbon atoms or an alkenyl group, R8 is a hydrogen atom, or ii is a linear alkyl group having 1 to 8 carbon atoms.) This whitening powder cosmetic is characterized in that at least one of the esters represented by (an alkyl group, an alkenyl group, n is an integer of 1 to 13) is blended together with an immobilized enzyme.

不発りjにおいて、美白剤成分(活性成分)として使用
されるエステル(モノエステルまたけジエステル〕は、
前記一般式で表わされる化合物である。このエステルは
、直鎖状の脂肪族飽和二塊基酸(炭素数3〜15)と直
鎖状の脂肪族飽和〜価アルコールとからなるモノエステ
ルまたはジエステルである。その構造は直鎖状で、分岐
鎖が無く、かつアルキル基またけアルケニル基の鎖長#
′i炭素&1〜8の比較的短かいこと等によって特徴づ
けられる。
The ester (monoester and diester) used as a whitening agent component (active ingredient) in Fubari J is
This is a compound represented by the above general formula. This ester is a monoester or diester consisting of a linear aliphatic saturated dicarboxylic acid (having 3 to 15 carbon atoms) and a linear aliphatic saturated to alcohol. Its structure is linear, without branching, and the chain length of the alkyl group and alkenyl group is #
It is characterized by its relatively short length of carbon 'i & 1 to 8.

本発明の前記一般式で表わされるエステルの中で、最も
好ましいものとしては、例えばアジピン酸、ピメリン酸
、スペリン酸、アゼライン酸、セ/<E/ン酸、1.9
−/ナメチレンジカルボン酸、1゜10−デカメギレン
ジカルボン酸等のモノメチルエステル、モノエチルエス
テル、モノアリルエステル、モノグチルエステル、モノ
アリルエステル、モノ−2−へダテニルエステル、ジメ
チルエステル、ジエチルエステル、ジアリルエステル、
シフ’ fルエステル、ジアリルエステル、ジアリルエ
ステル、ジー2−fテニルエステル、シー3−へキセニ
ルエステル、等が例示される。
Among the esters represented by the above general formula of the present invention, the most preferable ones are, for example, adipic acid, pimelic acid, superric acid, azelaic acid, se/<E/enoic acid, 1.9
-/monomethyl ester, monoethyl ester, monoallyl ester, monobutyl ester, monoallyl ester, mono-2-hedatenyl ester, dimethyl ester, diethyl ester of nameethylene dicarboxylic acid, 1゜10-decamethylene dicarboxylic acid, etc. , diallyl ester,
Examples include Schif'f ester, diallyl ester, diallyl ester, di2-f tenyl ester, and di3-hexenyl ester.

本発明において使用される固定化酵素とけ、プロテアー
ゼ、アミラーゼ等の酵素を実質的に水不溶性の担体に固
定化したものを言い、水不溶性の担体としては、例えば
ゼイン、シルクフィブロイン、カゼイン等の蛋白質、ア
ルギン酸、カルボキシメチルセルローズ等の多糖類、ア
クリルアミドゲル等の合成高分子等がある。これらの中
でも化粧料用として安全性の面より好適なものはカゼイ
ン、ゼイン、シルクフィブロイン、アルギン酸、カルボ
キシメチルセルローズ等の天然高分子中米のもの(天然
高分子およびその誘導体)である。
The immobilized enzyme used in the present invention refers to an enzyme such as protease, protease, amylase, etc. that is immobilized on a substantially water-insoluble carrier. Examples of the water-insoluble carrier include proteins such as zein, silk fibroin, and casein. , alginic acid, polysaccharides such as carboxymethyl cellulose, and synthetic polymers such as acrylamide gel. Among these, natural polymers from Central America (natural polymers and derivatives thereof) such as casein, zein, silk fibroin, alginic acid, and carboxymethyl cellulose are preferable for use in cosmetics in terms of safety.

また、本発明に使用する固定化酵素に固定化(含有)さ
れている酵素としてはプロテアーゼ、アミラーゼ等の加
水分解酵素が好ましく、特にプロテアーゼが良好な効果
を示す。
Furthermore, as the enzyme immobilized (contained) in the immobilized enzyme used in the present invention, hydrolytic enzymes such as protease and amylase are preferable, and protease shows particularly good effects.

包括法としては、例えばトウモロコシ蛋白ゼインの水性
溶液に酵素を渭合し、ゲル化して不溶化させたり、カゼ
インンーダの水溶液に酵素を混合しPHを酸性にしてカ
ゼインを沈澱形成させたりして、包括型の固定化酵素を
得ることができる。
Examples of comprehensive methods include, for example, combining an enzyme with an aqueous solution of corn protein zein and making it insoluble by gelling it, or mixing an enzyme with an aqueous solution of casein powder and making the pH acidic to form a precipitate of casein. of immobilized enzyme can be obtained.

また担体結合法としては通常の方法が用いられ、例えば
カルボキシメチルセルローズをメチル化シ、ヒドラジン
を作用せしめヒドラジドとし、更に亜硝酸を作用させて
酸アミド誘導4本とし、これに酵素を反応させることに
より、担体結合型の固定化酵素が得られる。
Further, a conventional method is used for carrier binding, for example, carboxymethyl cellulose is methylated, treated with hydrazine to form a hydrazide, further treated with nitrous acid to form four acid amides, and reacted with an enzyme. In this way, a carrier-bound immobilized enzyme can be obtained.

また酵素同士を結合させる架橋法としては通常の方法、
例えばトリレンジインシアネート、キシレンジインシア
ネート等の少なくとも二つ以上の官能性基を有する試薬
で酵素を架橋化処理することによって架橋型の固定化酵
素を得ることができる。
In addition, as a cross-linking method to bond enzymes together, the usual method,
For example, a crosslinked immobilized enzyme can be obtained by crosslinking the enzyme with a reagent having at least two or more functional groups, such as tolylene diinocyanate or xylene diinocyanate.

以上の固定化酵素のうちで好ましいものけ蛋白質等の天
然高分子にプロテアーゼ、アミラーゼ等を包括法で固定
化したものである。その中でもトクモロコシ蛋白のゼイ
ンにプロテアーゼを包括したものが、その酵素安定性、
保存安定性、安全性の上から特に好ましい。
Among the above-mentioned immobilized enzymes, preferred are those in which protease, amylase, etc. are immobilized on natural polymers such as Mononoke protein by an inclusive method. Among them, the horse mackerel protein zein containing protease is known for its enzyme stability.
Particularly preferred from the viewpoint of storage stability and safety.

本発明の前記エステルは、遊離二塩基酸に較べて角質蛋
白との結合性が低く、また皮脂に溶解しやすい利点を有
し、かつ固定化酵素を組み合わせることによって、前記
エステル単独よりも一層皮内浸透性が高まる。
The ester of the present invention has the advantage that it has a lower binding property with corneum proteins than a free dibasic acid and is easily dissolved in sebum, and when combined with an immobilized enzyme, it is more effective than the ester alone. Increases internal permeability.

これらの特性によって、本発明の美白化粧F)はチロシ
ナーゼ活性の阻害効果が著しく高く、優れた美白効果を
発、現しj(する。これらの特性、効果は例えばアナン
イシ酸、アジピン酸等の遊離の二塩基酸(特1ん昭53
−130446号片や例えばジイン10ピルアジペート
、ジー2−エチルへキシルアジペート等の分岐エステル
〔特公昭45−22435号)には見られないところで
あって、その特異性は著しい。
Due to these properties, the whitening cosmetic F) of the present invention has an extremely high inhibitory effect on tyrosinase activity and exhibits an excellent whitening effect. Dibasic acid (Special 1, 1984)
130446 and branched esters such as diyne-10-pyru adipate and di-2-ethylhexyl adipate (Japanese Patent Publication No. 45-22435), its specificity is remarkable.

本発明の美白化粧料における、前記一般式で表ワサれる
エステル(モノエステル、ジエステル)の少なくとも一
つの配合量は、美白化粧料の形態(種類)によって異な
るけれども、総括的な配合量は、当該化粧料の処方成分
全景を基準さして(以F同様)通常10〜25重量%(
好ましくけ12〜20重量%)の範囲内である。また本
発明の前記のモノエステルとジエステルを併用する場合
の両者の沖合割合け、100:O−0:100C1jf
iしくけ95:5〜5:95)である。
Although the amount of at least one of the esters (monoester, diester) represented by the above general formula in the whitening cosmetic of the present invention varies depending on the form (type) of the whitening cosmetic, the overall amount Based on the entire prescription ingredients of cosmetics (hereinafter the same as F), it is usually 10 to 25% by weight (
It is preferably within the range of 12 to 20% by weight). Further, when the monoester and diester of the present invention are used together, the offshore ratio of both is 100:O-0:100C1jf
i Shikke 95:5 to 5:95).

本発明に使用する固定化酵素さしては、酵素含有率が通
常5.0〜20重景%のものが適用される。
The immobilized enzyme used in the present invention usually has an enzyme content of 5.0 to 20%.

本発明の粉末化柱層における固定化酵素の配合量(使用
量)は、固定化酵素に含有している酵素量として、処方
成分全量に対して0.025〜2重景%、好ましくは0
1〜1N景%である。0.025重景%未満では酵素の
効果が低トし、2重量%をこえると顔面塗布時に著しい
異和感を与えやすい。
The blending amount (amount used) of the immobilized enzyme in the powdered columnar layer of the present invention is 0.025 to 2%, preferably 0.025% to 2%, based on the total amount of prescription ingredients, as the amount of enzyme contained in the immobilized enzyme.
It is 1-1N view%. If it is less than 0.025% by weight, the effect of the enzyme will be low, and if it exceeds 2% by weight, it will likely give a noticeable discomfort when applied to the face.

本発明に使用する固定化酵素は、粉末状であることが必
要で、通常、平均粒径が0.5〜20μのものが適用さ
れる。
The immobilized enzyme used in the present invention needs to be in powder form, and usually has an average particle size of 0.5 to 20 μm.

本発明の粉末状の美白化粧料は、デンプン、デキストリ
ン、カルボキシメチルセルローズ、ヒドロキシエチルセ
ルローズ、ヒドロキシグロビルセルローズ、ポリビニル
アルコール、ポリビニルビロドリン、カゼイン、セリシ
ン、乳糖、マンニツト、沈p$炭耐力ルシクム等の慣用
粉末基材に、本発明の前記エステル(モノエステルおよ
び/またはジエステルノと11j記固定化酵素を添加し
、均一に混練することによって製造される。
The powdered whitening cosmetic of the present invention contains starch, dextrin, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxyglobil cellulose, polyvinyl alcohol, polyvinyl birodrin, casein, sericin, lactose, mannitol, precipitated charcoal-bearing lucicum, etc. It is produced by adding the ester (monoester and/or diester) of the present invention and the immobilized enzyme described in 11j to a conventional powder base material, and uniformly kneading the mixture.

本発明の美白粉末化粧料け、パック、マツサージクリー
ム、寸だFi洗顔クリーム等の化tp+と9Fの如く混
線後通常使用法により用いられる。すなわち、木兄ゆj
の美白粉末化粧F11vを59のバッタ、マツサージク
リームまたけ洗顔クリームに練り込み、被験との顔面に
塗布する。バックの場合け゛約10分〜15分間塗布放
置0J1顔面より剥離する。77づ−ジクリームの場合
は、塗布後、&間開肌にすり込む様にマツサージをくり
返し、その後ティッシュペーパーまたは脱脂綿等でふき
とる。1だ、洗顔クリームの場合は、塗布後、顔面全体
を十分こする様Cでして況顔し、十分水洗いする。以上
の様Cて、本発明の美白粉末化粧料は一定量、化粧品1
・二M合され、一定時間肌に塗布処理後、ティッシュペ
ーパーまたは脱脂綿等でふき取られるか、洗い落とされ
る様な方法で使用される。
The skin whitening powder cosmetics of the present invention, packs, pine surge cream, Sunda Fi facial cleansing cream, etc., can be used according to the normal usage method after mixing, such as tp+ and 9F. In other words, Kien Yuj
Whitening powder makeup F11v is mixed into 59 grasshopper, pine surge cream, and facial cleansing cream, and applied to the face of the test subject. For back skin, leave it on for about 10 to 15 minutes and peel off from the face. In the case of 77zu-di cream, after applying it, rub it into the open skin repeatedly and then wipe it off with tissue paper or absorbent cotton. 1. In the case of facial cleansing cream, after applying it, rub the entire face thoroughly with C, then rinse thoroughly with water. As described above, the whitening powder cosmetic of the present invention can be used in a certain amount as cosmetic 1.
・It is used in such a way that it is mixed with two M, applied to the skin for a certain period of time, and then wiped off with tissue paper or absorbent cotton, or washed off.

以ド木発明を実施例によって詳述する。尚、実施例に示
す部とけ重量部を意味する。寸だ、酵素古性率(活性保
持率]、感触、経日安定ヤ↓け後述のlli!、M法に
よって調べた。
The invention will now be described in detail with reference to examples. Incidentally, the parts shown in Examples refer to parts by weight. The enzyme aging rate (activity retention rate), feel, and stability over time were investigated using the LLI! and M methods described below.

プロテアーゼ活性測定試験法 p−トシルアルギニンメチルエステル0.033M水溶
液(PH8)中に適当量の固定化プロテアーゼを含有す
る試料を加え、60℃で30分間攪拌しながら反応させ
た後、Iooorpmで5分間遠心し、上澄液を採り、
ガスクロマトグラフィーにより活性を測定する。保存開
始時および一定期間保存後の活性を測定し、以Fの式よ
り活や1−保持率を磐田する。
Protease activity measurement test method A sample containing an appropriate amount of immobilized protease was added to a 0.033M aqueous p-tosylarginine methyl ester solution (PH8), reacted at 60°C for 30 minutes with stirring, and then at Iooorpm for 5 minutes. Centrifuge, collect the supernatant,
Activity is determined by gas chromatography. The activity at the start of storage and after storage for a certain period of time is measured, and the activity and 1-retention rate are calculated using the following formula.

Oアミラーゼ活性測定試験法 デンプン水溶液に適当量の固定化アミラーゼを含有する
試料を加え攪拌をしながら30℃、60分同反応した後
、生成した還元性糖を過マンガン酸カリウム溶液で定量
して求める〜 Eてついて基間べた。
Test method for measuring O-amylase activity: Add a sample containing an appropriate amount of immobilized amylase to an aqueous starch solution, react with stirring at 30°C for 60 minutes, and then quantify the reducing sugars produced using a potassium permanganate solution. I'm looking for ~ I asked E and asked Motoma.

′!2だそれぞれの美白粉末を処方の/(ツク(皮膜!
1.9 )化粧トI−の中に加えて混線後、顔に塗布し
た時の実用特性(感触)を調べた。
′! 2. Each skin whitening powder is prescribed / (Tsuku (film!
1.9) The practical characteristics (feel) when applied to the face after mixing with the makeup product I- were investigated.

次に1〆4定化酵素の調製法を示す。Next, a method for preparing the 1〆4-containing enzyme will be described.

長瀬産業裂プロテアーゼまたけアミラーゼをそれぞれ次
の方法で固定化し、てJl”、]製した(なお混合比率
F1g累:担体=1:4)。
Nagase Sangyo Protease Protease Amylase was immobilized by the following method to prepare a product (mixing ratio F1g: carrier = 1:4).

クゼイン固定化70テアーセ゛(Z工P)トウモロニア
 E/ 蛋白セ゛イン金イソプロピルアルコールで抽出
しプロテアーゼ°を添加後、攪拌しながら、水を添加し
て沈澱せしめ乾燥、粉砕して調製する7、 Oゼイン固定化アミラーゼ(Z工A) Z工Pと同方法で調製する。
70 Teasein Immobilization (Z Engineering P) Toumoronia E/Protein Sein Extract with gold isopropyl alcohol, add protease °, add water while stirring, precipitate, dry and grind to prepare 7.Ozein fixation amylase (Z-A) Prepared in the same manner as Z-A.

O絹フィブロイン固定化グロテアーゼ(rrxp)約フ
ィブロインを銅エチレンジアミンに溶解し、透析し、銅
工手レンジアミンを除去後プロテアーゼを添加し、攪拌
しながら硫安を加えて塩析して沈澱せしめ、乾燥、粉砕
して調製する。
Silk fibroin immobilized grotease (rrxp) About fibroin was dissolved in copper ethylene diamine, dialyzed, and after removing the copper diamine, protease was added, and while stirring, ammonium sulfate was added to precipitate by salting out, and then dried. Prepare by grinding.

6mフィブロイン固定化アミラーゼ(IFIA)FTP
と同方法で調製する Oカルボキシメチルセルロース固定化10テアーセ゛ カルポキンメチルセルロースナトリクムヲ水に溶解し、
それ(てプロテアーゼを加え火に塩化カルシツムを添加
して、沈澱を生しめしめ、乾燥、粉砕して調製する。
6m fibroin-immobilized amylase (IFIA) FTP
O-carboxymethylcellulose immobilized 10-tear carpoquine methylcellulose sodium prepared in the same manner as above was dissolved in water,
It is prepared by adding protease and adding calcium chloride to the mixture to form a precipitate, then drying and crushing it.

o 7 ルギン酸固定化グロテアーセ゛アルギン酸ナト
リクムを水に溶解し、それにグロテアーゼ乞加え、更に
酸を加えてPI(を4以トとして沈澱を生じせしめ、乾
燥、粉砕して調製する。
o 7 Sodium alginate, a grotease immobilized with ulginic acid, is dissolved in water, grotease is added thereto, an acid is added thereto, PI (4 or more) is added to form a precipitate, and the precipitate is prepared by drying and pulverizing.

リアクリルア三ドデル固定化プロテアーセ゛アクリルア
ミドモノマー、N、N’−メチレンビスアクリルアミド
およびプロテアーゼを緩衝液に溶解し、これに重合促進
剤としてβ−ジメチルア三ノプロピオニトリルおよび重
合開始剤トして、K2S、03を加えて重合反応ケ行な
い調製する。
Immobilized protease: Acrylamide monomer, N,N'-methylenebisacrylamide and protease are dissolved in a buffer solution, and β-dimethylamitrinopropionitrile as a polymerization accelerator and a polymerization initiator are added to K2S, 03 was added to carry out the polymerization reaction.

o美白効果の/ζネルテスト 実施例1.2捷たけ6およびそれぞれの比較例の美臼化
叡1)(・粉末1vをF記処方の皮膜型・ζツク剤52
中に練り込み、被験者の顔面に毎日朝夕1回宛の塗布を
4ケ月間くり返して美白効果を比較した。ただし、実施
例4についてrf′ii!D続塗布2.4.6ケ月後に
おいて美白効果を経口的に比較した。
o Skin whitening effect/ζ skin test Example 1.2 Katsutake 6 and each comparative example of Beauty Usage 1) (・Powder 1 vol.
The skin whitening effect was compared by kneading it into the skin and applying it once a day in the morning and evening to the subjects' faces for four months. However, regarding Example 4, rf′ii! After 2, 4 and 6 months of continuous application of D, the whitening effect was compared orally.

尚、被事験者は各群20名とし、かつシミ、ソバカス、
色黒の悩みを有する人を対象とした。
In addition, there were 20 subjects in each group, and there were no age spots, freckles,
Targeted at people who suffer from dark skin.

効果のあったパネラ−数とは、良いおよびやや良いに相
当する被検者の総数であるっ 一方、実施例4あ・よび各比較例の美白化粧お1粉末1
vをF&I処方のマツサージクリーム57の中にまた実
施例5および各比較例の美白粉末化粧料17をド記処方
の洗顔クリーム5gの中に練り込み、それぞね2[]名
の被験者が通常の方法で毎日朝夕1回宛の塗布を4ケ月
間くり返して美白効果を同様に比較した。
The number of panelists who had an effect is the total number of subjects who rated it as good and fair.
V was kneaded into pine surge cream 57 prescribed by F&I, and whitening powder cosmetic 17 of Example 5 and each comparative example was kneaded into 5 g of facial cleansing cream prescribed by Do. The whitening effect was similarly compared by applying the same method once a day in the morning and evening for four months.

0皮膜型パツク剤の処方 ポリビニルアルコール           15州4
エタノール                15部グ
リセリン               5部カオリン
                5部香  料   
                 01部メチル/(
クベン              01部水    
                       59
8都総  量                   
 100部マッザージクリームの処方 パラフィン              40部マイク
ロクリスタリンワックス           60部
ミツロ!7                60部ワ
セリン                 +4.0部
流動パラフィン            425部ンル
ビタンセスキオレイン酸エステル        3.
7 ff1(ポリオキシエチレンンルビタン     
  08部七ノオレイン酸エステル(20g、o、)メ
チルノζラベン               02都
香  料                    0
1部水                      
      227部総 量      100部 ・洗顔クリームの処方 流動ノリフィン            ′55 部オ
シクライト                8 部パ
ラフィン                 5 部コ
レステロール              6 部中ス
キオレイン酸ンルビクン        1.5部モノ
オレイン酸ポリオキシ エチレンソルビクン(20ε、o、)      [1
,3mメチルパラベン              0
1都香   P)                 
       0.1部水             
               47、D部総 量  
          +00.0部第2表に示す。
0 Film type pack formulation Polyvinyl alcohol 15 states 4
Ethanol 15 parts Glycerin 5 parts Kaolin 5 parts Fragrance
01 parts methyl/(
Kuben 01 part water
59
Total amount of 8 cities
100 parts massage cream prescription paraffin 40 parts microcrystalline wax 60 parts Mitsuro! 7 60 parts Vaseline + 4.0 parts liquid paraffin 425 parts Rubitan sesquioleate 3.
7 ff1 (polyoxyethylene rubitan
08 parts heptanooleic acid ester (20g, o) methylnolaben 02 Miyako fragrance 0
1 part water
227 parts Total amount 100 parts Facial cleansing cream prescription Liquid Norifin '55 parts Ocyclyte 8 parts Paraffin 5 parts Cholesterol 6 parts Rubicun schioleate 1.5 parts Polyoxyethylene sorbicun monooleate (20ε, o,) [1
,3m Methylparaben 0
1 Miyako P)
0.1 part water
47. Total amount of D part
+00.0 parts shown in Table 2.

調製法: 後記の第2表に示す処方成分の(1)、(4)に酵素、
固定化酵素(酵素含料10%ン、2塩基酸エステル又は
そのMlみ合わしたものをそれぞれ添加し、均一に混合
攪拌する。一方、成分(2)と(6)を均一番で混合攪
拌する。
Preparation method: Enzyme,
Add immobilized enzyme (enzyme content 10%, dibasic acid ester, or its Ml) and mix and stir uniformly.Meanwhile, mix and stir components (2) and (6) in uniform numbers. .

その後、両組酸物を混合し、再度均一に混合槽拌して篩
を通し調製した。
Thereafter, both sets of acid substances were mixed, uniformly stirred in the mixing tank again, and passed through a sieve.

この粉末美白化粧料け45℃、4ケ月間保存し、それぞ
れの製品中の酵素活性の安定性を測定した。
The powder whitening cosmetics were stored at 45°C for 4 months, and the stability of the enzyme activity in each product was measured.

寸だ木美白化粧F)の使用時の感触及び美白効果を第2
表に示した。
The feel and whitening effect of Sundaki Whitening Makeup F) during use are as follows:
Shown in the table.

相応を与え、また0、05重景%以ドの場合け、美白効
果がほとんど期待されない。
If the concentration is less than 0.05%, almost no whitening effect can be expected.

基剤中に2塩基酸エステルとして、アゼライン酸ジエチ
ルを15重景%と固定化酵素(Z工P又けZIA)を0
,05〜5.0重量%を配合した美白化粧料の美白効果
は著しく、また官能効果(皮膚の果の特異性は著しい。
As a dibasic acid ester in the base, 15% diethyl azelaate and 0% immobilized enzyme (Z Engineering P Matake ZIA) were added.
, 05 to 5.0% by weight, the whitening effect is remarkable, and the sensory effect (specificity of skin effects is remarkable).

粧刺、又は、基剤中に固定化酵素(2工P又はZ工A)
のみを配合した粉末化粧料の美白効果は著しく低かった
Immobilized enzyme in cosmetic stitch or base (2-tech P or Z-tech A)
The whitening effect of powdered cosmetics containing only the following was extremely low.

発クツの美白化粧Nに比較すれば、その効果は満足合の
酵素活性の安定性を測定した結果、いずれの場合も固定
化酵素を配合した試料中の酵素活性は低トしなかったが
、未固定酵累を配合した試料中の酵素活性は著しく低ト
し、着色が認められた。
Compared to Hakkutsu's Whitening Cosmetics N, the effect was satisfactory.As a result of measuring the stability of enzyme activity, in both cases, enzyme activity in samples containing immobilized enzymes did not decrease; The enzyme activity in the sample containing unfixed yeast mixture was significantly reduced and coloration was observed.

3表に示す。It is shown in Table 3.

調製法: 後記の第6表に示す処方成分の(1)、(31、(4)
に酵素、固定化酵素、2塩基酸エステルまたけその絹み
合わ也たものを、それぞれ添加し、均一に混合攪拌する
。−力、成分(2)と(5)を均一に混合攪拌する。
Preparation method: Prescription ingredients (1), (31, (4) shown in Table 6 below)
Enzymes, immobilized enzymes, dibasic acid esters, and a combination of the same are added to the mixture, and the mixture is uniformly mixed and stirred. - Mix and stir ingredients (2) and (5) uniformly.

その後、両組酸物を混合し、再度均一に混合攪拌して、
篩を通し1.IJ製した。
After that, both sets of acids were mixed and stirred uniformly again.
Pass through a sieve 1. Manufactured by IJ.

この粉末美白化粧料H45℃、4ケ月間保存し、それぞ
れの製品中の酵素活性の安定性を測定した。
This powder whitening cosmetic product was stored at 45° C. for 4 months, and the stability of the enzyme activity in each product was measured.

また木美白化粧料の使用時の感触および美白効果を第6
表に示した。
In addition, the feel and whitening effect when using wood whitening cosmetics were evaluated as
Shown in the table.

!2表より明らかなように、炭素&6〜15(■=1〜
13ンの2塩基酸ジエチルエステルのいずれか一種と固
定化酵、+1(ZIPJを組み合わせた粉末化粧料の美
白効果及び官能効果はいずれも顕著であった。一方、基
剤中に2塩基酔エステルのみを配合した粉末化粧料にけ
美白効果が認められたが、本発明の美白化粧料に比較す
ればその効果#−tfi足すべきものではなかった。
! As is clear from Table 2, carbon &6~15 (■=1~
Both the whitening effect and the sensory effect of the powder cosmetics containing one of the dibasic acid diethyl esters of 13N, immobilized yeast, and +1 (ZIPJ) were remarkable. Although a whitening effect was observed in the powdered cosmetic containing only the whitening cosmetic of the present invention, the effect was not as good as that of the whitening cosmetic of the present invention.

また、基剤中に固定化酵素(Z工P)のみを配合した粉
末化粧料及び粉末基剤にけ美白効果が認効果の特異性は
著しい。
In addition, the whitening effect of the powder cosmetic containing only the immobilized enzyme (Z-P) and the powder base has remarkable specificity.

各粉末美白化粧料を45℃、4ケ月間保存した場合のM
、素活性の安定性を測定した結果、いずれの場合も固定
化酵素を配合した試料中の酵素活性け実施例6 粉末美白化粧料(美白・−クダー)の調製処方は第4表
に示す。
M when each powder whitening cosmetic is stored at 45℃ for 4 months
As a result of measuring the stability of the elementary activity, in each case, the enzyme activity in the sample containing the immobilized enzyme was determined.Example 6 Table 4 shows the formulation for the preparation of powder whitening cosmetics (whitening/Kuda).

調製法: 後記の第4表に示す処方成分の(1)、(4)に酵素、
固定化酵素、2塩基酸エステル又はその組み合わしたも
のをそれぞれ添加し、均一に混合攪拌する。
Preparation method: Enzyme,
An immobilized enzyme, a dibasic acid ester, or a combination thereof is added, and the mixture is mixed and stirred uniformly.

その後、両組酸物を混合し、再度均一にM召攪拌して、
篩を通し調製した。
After that, both sets of acids were mixed and stirred uniformly again.
Prepared by passing through a sieve.

この粉末美白化粧Pけ45℃、4ケ月間保存し、それぞ
れの製品中の酵素活性の安定性を測定した。
This whitening powder powder was stored at 45°C for 4 months, and the stability of the enzyme activity in each product was measured.

また木矢白化粧料の使用時の感触及び美白効果を第4表
に示した。
Table 4 also shows the feel and whitening effect of Kiyawhite cosmetics when used.

第6表の結果から明らかなよう((、炭素数1〜8のア
ルキル基又はアルケニル基の2塩基酸エステルのいずれ
み一種と固定化酵素(ZIP)を組み合わせた粉末化粧
料の美白効果及び官能結果はいずれも顕著であった。一
方晶剤中(て2塩基酸エステルのみを配合した粉末化粧
トドにけ美白効果が認められたが、本発明の美白化粧料
に比較すれば、その効果は満足すべきものでけなかった
。また基剤中に固定化酵素(ZIP)のみを配合した粉
末化粧料及び粉末基剤にけ美白効果が認められなかった
0 票 以上の結果により、本発明粉体美白化粧料の作用効果の
特異性は著しい。尚、炭素数9以上のアルキル基又はア
ルクール基の2塩基酸エステルを配合した粉末化粧料の
美白効果は十分満足すべきものではなかった。
As is clear from the results in Table 6, the whitening effect and sensory effects of powdered cosmetics in which any dibasic acid ester of an alkyl group or alkenyl group having 1 to 8 carbon atoms is combined with an immobilized enzyme (ZIP) are All the results were remarkable.On the other hand, the whitening effect was observed in the powdered makeup containing only the dibasic acid ester in the crystallizer, but when compared to the whitening cosmetic of the present invention, the effect was lower. Furthermore, the whitening effect was not observed in powder cosmetics containing only immobilized enzyme (ZIP) in the base and in the powder base.The result of 0 votes or more indicates that the powder of the present invention The specificity of the action and effect of whitening cosmetics is remarkable.The whitening effect of powdered cosmetics containing a dibasic acid ester of an alkyl group or an alcohol group having 9 or more carbon atoms was not fully satisfactory.

各粉末美白化粧料を45℃、4ケ月間保存した場合の酵
素活性の安定性を測定した結果、いずれの場合も固定化
酵素を配合した試刺中の酵素活性は実施例4 粉末美白化粧料(美白/曵りグー)の調製処方は第5表
に示す。
As a result of measuring the stability of enzyme activity when each powdered whitening cosmetic was stored at 45°C for 4 months, the enzyme activity in the sample containing immobilized enzyme was found to be Example 4 Powdered whitening cosmetic The preparation recipe of (Whitening/Hirikuri Goo) is shown in Table 5.

調製法: 後記の第5表に示す処方成分の(1)、(4)に酵素、
固定化酵素、2塩基酸エステIし又けその組入合わした
ものをそれぞれ添加し、均一に度合攪拌する0一方、成
分(2)と(3)を均一に混合W!痒する。
Preparation method: Add enzymes to (1) and (4) of the prescription ingredients shown in Table 5 below.
Add the immobilized enzyme and the combination of dibasic acid ester I Shimata Keso and stir uniformly.Meanwhile, components (2) and (3) are uniformly mixed W! Itches.

その彼、両組酸物を混合し、再度均一にM合jgt件し
て、篩を通し調製した。
Then, the two sets of acids were mixed together, uniformly mixed again, and passed through a sieve to prepare the mixture.

この粉末美白化粧料は45℃、4ケ月(帛保存し、それ
ぞれの製品中の酵素活性の安定性を測定した。
This powder whitening cosmetic was stored at 45°C for 4 months, and the stability of the enzyme activity in each product was measured.

また木美白化粧料の使用時の感触及び美白効果を第5表
に示した3、 第5表の結果からりjらかなように、2塩基酸エステル
(アゼライン酸ジエチlレエステル〕とbI定イし酵素
(zrp)を組み合わせた本発明の粉末イヒ粧料(粉末
]】は2ケ月後、美白効果ありと答えたノζネラー数が
20名甲乙名に認められ、4ケ月後で15名、6ケ月律
17名と著しい美白効果の増大を示した。
Table 5 also shows the feel and whitening effect of the wood whitening cosmetic when used.3 From the results in Table 5, it is clear that dibasic acid ester (diethyl azelaic acid ester) and bI constant After 2 months, 20 people answered that the powdered cosmetics (powder) of the present invention combined with the enzyme (ZRP) had a whitening effect, and after 4 months, 15 people answered that it had a whitening effect. It showed a significant increase in the whitening effect with 17 patients taking six months.

それにス・1し、基剤中に2塩基酩エステル(アゼライ
ン酸ジエチルエステル)のみを配合した粉末化粧PI 
(粉末スノの場合は、連続塗布4ケ月後Cて美白9JJ
果の、窮められたパネラ−#け、70名巾計名、6ケ月
後は20名巾計6名であった。fi’l] 、木発すj
の粉末 は比較例の粉末ユよりも美白効果の発現が著し
く連やかであり、冨能効果面でも秀れていることはqI
白である。
Powder cosmetic PI containing only 2-base alcohol ester (azelaic acid diethyl ester) in addition to S.1.
(In the case of powder snow, apply whitening 9JJ after 4 months of continuous application.)
As a result, there were 70 panelists in total, and 6 months later, there were 20 panelists in total, with a total of 6 members. fi'l]
The whitening effect of the powder was significantly longer than that of the comparative powder Yu, and the fact that it was also superior in terms of the tonicity effect is qI.
It is white.

一方、基剤中に遊離2塩基酸(アゼライン酸)のみ全配
合した粉末化粧PI (粉末4)、および基剤中に遊離
2塩基酸(アゼライン酸うと固定化酵素〔2IPJを配
合した粉末化粧)1(粉末g)の美白効果の発現は速や
かでなく、その効果も十分満足すべきもので行ない。
On the other hand, powder cosmetic PI (powder 4) which contains only free dibasic acid (azelaic acid) in the base, and powder cosmetic containing free dibasic acid (azelaic acid and immobilized enzyme [2IPJ) in the base] The whitening effect of No. 1 (powder g) did not appear quickly, and the effect was sufficiently satisfactory.

更に、基剤中に固定化酵素(ZIP)のみを配合した粉
末化粧料(粉末3)、及び粉末基剤(粉末ら)に#−を
美白効果けほとんど認められなかった。
Furthermore, in the powder cosmetic containing only the immobilized enzyme (ZIP) in the base (Powder 3) and in the powder base (Powder et al.), almost no whitening effect was observed in #-.

以上の結果より、本発明の粉末美白化粧料(粉末1)の
作用効果の特異性は著しい。
From the above results, the specificity of the action and effect of the powder whitening cosmetic (powder 1) of the present invention is remarkable.

実施例5 粉末美白化粧料〔美白バクグー〕の調製処方は第6表に
示す。
Example 5 Table 6 shows the preparation recipe of powdered whitening cosmetics [Whitening Bakugou].

調製法: 移記の第6*に示す処方成分の(1)、(4)に酵素、
固定化酵素、2塩基酸エステル又はその組み合わしたも
のをそれぞれ添加し、均一(で混合投畔する。
Preparation method: Enzyme,
Immobilized enzymes, dibasic acid esters, or a combination thereof are added and mixed uniformly.

一方、成分(2)と(6)を均一に胛合攬畔する。Meanwhile, components (2) and (6) are uniformly combined.

その後、両組酸物を混合し、再度均一に混合4)1拌し
て、篩を通し調製した。
Thereafter, both sets of acid compounds were mixed, uniformly mixed again (4), stirred, and passed through a sieve.

この粉末美白化粧P1は45℃、4ケ月間保存し、それ
ぞれの製品中の酵素活性の安定性を測定した。
This powder whitening makeup P1 was stored at 45°C for 4 months, and the stability of enzyme activity in each product was measured.

また木美白化粧料の使用時のE5触及ブ美白効果を第6
表に示した。
In addition, the 6th whitening effect of E5 when using wood whitening cosmetics.
Shown in the table.

第6麦の結果から明らかなように、2壌基酸エステル(
1,9−ノナメチレンジカルボン酸エステル効果及び官
能効果はいずれも顕著であった。一方、2Jm基酸=ス
テル(1,9−/ナメチレンジ力ルボン酸エステル−ジ
−n−グチル)と未固定酵素(プロテアーゼ又はアミラ
ーゼ)を組み合わせた粉末化粧料の美白効果及び官能効
果はいずれも十分満足するものではなかった。
As is clear from the results for No. 6 wheat, disodium base acid ester (
Both the 1,9-nonamethylene dicarboxylic acid ester effect and the sensory effect were significant. On the other hand, the whitening effect and sensual effect of powdered cosmetics that combine 2Jm base acid = ster (1,9-/namethylene dicarboxylic acid ester - di-n-butyl) and unimmobilized enzyme (protease or amylase) are sufficient. It wasn't satisfying.

また、基剤中に2塩基酸エステルのみを配合17た粉末
化粧P1についても、その美白効果を認めるものの本発
明の美白化粧判に比較すれば、その効果は満足すべきも
のではなかった。
Further, although powder cosmetic P1 containing only dibasic acid ester in the base was found to have a whitening effect, its effect was not satisfactory when compared to the whitening cosmetic of the present invention.

更【C1基剤中に固定化酵素(FIP又けF工パノのみ
をrEi合した粉末化粧料の美白効果についてはその美
白効果は著しく低く、官能特性も悪かった。
Furthermore, regarding the whitening effect of a powdered cosmetic containing only an immobilized enzyme (FIP and F-Technol) in a C1 base, the whitening effect was extremely low, and the sensory properties were also poor.

各粉末チ白化粧刺・を45℃、4ケ月間保存した場合の
酵素活性の安定性を測定した結果、いずれの場合も、固
定化酵素を配合した試着の酵素活性吋95%以上で外観
の変化亀なかったのに対し、ツ固定酵素の場合は著しく
安定性に欠け、外観も着色を伴った。
As a result of measuring the stability of enzyme activity when each powdered Chihaku Makeshit was stored at 45℃ for 4 months, it was found that in all cases, the enzyme activity of the sample containing immobilized enzyme was 95% or more, resulting in a change in appearance. On the other hand, there was no change in the enzyme, whereas in the case of the fixed enzyme, the stability was markedly lacking and the appearance was also accompanied by coloration.

以上の結果より、2塩基酸エステルと固定化酵素を組み
合わせた本発明の粉末美白化粧料の作用効果の特異性は
著しい。
From the above results, the specificity of the action and effect of the powder whitening cosmetic of the present invention, which combines a dibasic acid ester and an immobilized enzyme, is remarkable.

Claims (1)

【特許請求の範囲】 (1)  美白剤成分として、ト記一般式%式% (上記式中で、R1け炭素数1〜8の直鎖状のアルキル
基またけアルケニル基、R2は水素原子または炭素数1
〜8の直鎖状のアルキル基あるいはアルケニル基であり
、nは1〜16の整数である。) で表わされるエステルの少なくとも一つが、固定化酵素
の粉末と共して配合されていることを特徴とする美白粉
末化粧料。 (2)  固定化酵素が、高分子物質からなる担体にプ
ロテアーゼまたけアミラー七゛が固定化されているもの
である特許請求の範囲第(1)項記載の美白粉末化粧料
。 (ろ) 前記一般式で表わされるモノエステルおよびジ
エステルの少なくとも一つが、当該化粧料の処方成分全
量を基準として10〜25重量%配合されている、特許
請求の範囲第(1)項記載の美白粉末化粧料。 (41fi!if定化酵素が、当該化粧料の処方成分全
量を基準として05〜10重量%西己含されている特許
請求の範囲第(1)項記載の美白粉末化粧料。 (5)固定化酵素が、固定化酵素中の酵素含有率が5〜
20重量%のものである、特許請求の範囲第(1)項記
載の美白粉末化粧料。
[Scope of Claims] (1) As a whitening agent component, the general formula % (%) (in the above formula, R1 is a linear alkyl group having 1 to 8 carbon atoms or an alkenyl group, and R2 is a hydrogen atom) or carbon number 1
~8 linear alkyl or alkenyl groups, and n is an integer of 1 to 16. A skin whitening powder cosmetic, characterized in that at least one of the esters represented by ) is blended together with an immobilized enzyme powder. (2) The whitening powder cosmetic according to claim (1), wherein the immobilized enzyme is one in which a protease-spanning amylyl 7 is immobilized on a carrier made of a polymeric substance. (b) The skin whitening according to claim (1), wherein at least one of the monoester and diester represented by the general formula is blended in an amount of 10 to 25% by weight based on the total amount of prescription ingredients of the cosmetic. Powder cosmetics. (The whitening powder cosmetic according to claim (1), in which the 41fi!if fixing enzyme is contained in an amount of 05 to 10% by weight based on the total amount of prescription ingredients of the cosmetic. (5) Fixation The enzyme content in the immobilized enzyme is 5~
The whitening powder cosmetic according to claim (1), which contains 20% by weight.
JP7991883A 1983-05-06 1983-05-06 Powdery makeup cosmetic Granted JPS59204114A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7991883A JPS59204114A (en) 1983-05-06 1983-05-06 Powdery makeup cosmetic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7991883A JPS59204114A (en) 1983-05-06 1983-05-06 Powdery makeup cosmetic

Publications (2)

Publication Number Publication Date
JPS59204114A true JPS59204114A (en) 1984-11-19
JPH0458442B2 JPH0458442B2 (en) 1992-09-17

Family

ID=13703671

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7991883A Granted JPS59204114A (en) 1983-05-06 1983-05-06 Powdery makeup cosmetic

Country Status (1)

Country Link
JP (1) JPS59204114A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2732593A1 (en) * 1995-04-04 1996-10-11 Bieurope Cosmetic for application to human skin
FR2848847A1 (en) * 2002-12-18 2004-06-25 Coletica COSMETIC OR DERMOPHARMACEUTICAL COMPOSITION COMPRISING AN AQUEOUS INSOLUBLE ENZYME AND USES THEREOF
US9226515B2 (en) 2004-02-03 2016-01-05 Cargill, Incorporated Protein concentrate and an aqueous stream containing water-soluble carbohydrates

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2732593A1 (en) * 1995-04-04 1996-10-11 Bieurope Cosmetic for application to human skin
FR2848847A1 (en) * 2002-12-18 2004-06-25 Coletica COSMETIC OR DERMOPHARMACEUTICAL COMPOSITION COMPRISING AN AQUEOUS INSOLUBLE ENZYME AND USES THEREOF
US9226515B2 (en) 2004-02-03 2016-01-05 Cargill, Incorporated Protein concentrate and an aqueous stream containing water-soluble carbohydrates
US10154679B2 (en) 2004-02-03 2018-12-18 Cargill, Incorporated Protein concentrate and an aqueous stream containing water-soluble carbohydrates

Also Published As

Publication number Publication date
JPH0458442B2 (en) 1992-09-17

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