JP2504064B2 - Cosmetics - Google Patents
CosmeticsInfo
- Publication number
- JP2504064B2 JP2504064B2 JP62192656A JP19265687A JP2504064B2 JP 2504064 B2 JP2504064 B2 JP 2504064B2 JP 62192656 A JP62192656 A JP 62192656A JP 19265687 A JP19265687 A JP 19265687A JP 2504064 B2 JP2504064 B2 JP 2504064B2
- Authority
- JP
- Japan
- Prior art keywords
- extract
- styrene
- resin
- crude drug
- adsorption resin
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8117—Homopolymers or copolymers of aromatic olefines, e.g. polystyrene; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
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)
- Cosmetics (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、生薬抽出物を微細孔を有する疎水性のスチ
レン系吸着樹脂に吸着せしめて生薬抽出物を安定に保つ
と共に、生薬抽出物を吸着した前記スチレン系吸着樹脂
を皮膚表面に接触させて使用するとき、皮膚表面の温度
及び水分、油溶性成分によって生薬抽出物が徐々にスチ
レン系吸着樹脂から溶出し、皮膚に対し生薬の持つ性能
が徐々に発揮されるようにした、スチレン系吸着樹脂を
配合してなる化粧料に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention makes a crude drug extract stable by adsorbing the crude drug extract on a hydrophobic styrene-based adsorption resin having fine pores, and When the adsorbed styrene-based adsorption resin is used in contact with the skin surface, the herbal medicine extract gradually elutes from the styrene-based adsorption resin due to the temperature and moisture of the skin surface and oil-soluble components, and the performance of the crude drug on the skin The present invention relates to a cosmetic composition containing a styrene-based adsorbent resin that is gradually exhibited.
従来、化粧料に用いられる生薬は、油脂類、脂肪酸、
脂肪酸エステル、アルコール類、水、炭化水素類等の溶
剤で抽出したものが用いられている。そして、この生薬
は、化粧料の剤型や効能、目的にあわせて単独もしくは
2種類以上が配合され直接皮膚に接触する状態で用いら
れる。Conventionally, crude drugs used in cosmetics include fats and oils, fatty acids,
Those extracted with solvents such as fatty acid esters, alcohols, water and hydrocarbons are used. This crude drug is used alone or in combination of two or more types according to the dosage form, efficacy and purpose of the cosmetic, and is used in a state of being in direct contact with the skin.
これらの生薬抽出物に含まれている成分は、精油成
分、サポニン類、タンニン酸類、アルカロイド類、糖
類、フラボノイド類等広範囲な成分の混合物からなり、
化粧品製剤中の各種の原料や空気、光、水分との接触等
により変化を受けやすい。これら生薬抽出物に含まれる
成分の変化は、製剤の変敗や沈澱物の生成凝集などとな
って現れ、化粧品製剤の安定性の上で問題を生じやす
い。The components contained in these crude drug extracts consist of a mixture of a wide range of components such as essential oil components, saponins, tannic acids, alkaloids, sugars, flavonoids,
It is susceptible to changes due to contact with various raw materials in cosmetic preparations, air, light, and moisture. Changes in the components contained in these crude drug extracts appear as deterioration of the preparation and formation and agglomeration of precipitates, which tend to cause problems in the stability of cosmetic preparations.
化粧料の内、洗浄剤類は、通常、界面活性剤もしくは
溶剤を多量に含有し、生薬抽出物の溶解度が増し、微粒
子として製剤中に存在するため、生薬成分は他の成分と
の接触面積が大きく、生薬成分以外の成分との反応を起
こしやすい。特に、酸やアルカリ性物質が製剤中に配合
されている場合には、これらの物質による変化を受けや
すい。更に、生薬抽出物が皮膚表面に高濃度に接触する
と、皮膚に炎症を起こすことがあり、低濃度で徐々に接
触させることが有効な場合が多い。Among cosmetics, detergents usually contain a large amount of surfactants or solvents, the solubility of the crude drug extract is increased, and they are present as fine particles in the formulation, so the crude drug component has a contact area with other components. Is large and easily reacts with components other than crude drug components. In particular, when an acid or alkaline substance is mixed in the preparation, it is likely to be changed by these substances. Further, when the herbal medicine extract is brought into contact with the skin surface at a high concentration, the skin may be inflamed, and it is often effective to gradually contact it at a low concentration.
洗浄剤の内、その製剤中に各種の粒子が配合されてい
るスクラブ剤が知られているが、このスクラブ剤に使用
される粒子としては、無機質や有機質のものを粉粒体と
して成型したものや、植物を破砕した粒状のもの、ある
いは特許第1346314号に記載されている球状のポリスチ
レン、ポリエチレン、ポリプロピレン、アクリル、ナイ
ロン等が知られている。Among cleaning agents, scrubbing agents in which various particles are mixed in the formulation are known, and the particles used in this scrubbing agent are inorganic or organic particles molded as powder particles. Also known are granular products obtained by crushing plants, and spherical polystyrene, polyethylene, polypropylene, acrylic, nylon, etc. described in Japanese Patent No. 1346314.
また、クリーム類、乳液類の製剤中に各種の球状粒子
を配合する場合もあるが、これは、クリーム類等の使用
時における伸びの改善や、滑らかさ等の感触の改良を目
的とすると共に、製剤中でつや消し効果を期待できる。
このような製剤に用いられる粒子としてはポリスチレ
ン、ポリエチレン、ポリプロピレン、ナイロン、アクリ
ル等のプラスチックからなる球状粒子が知られている。In addition, there are cases where various spherical particles are blended in the preparations of creams and emulsions, which aims to improve the elongation when using creams and the like, and to improve the feel such as smoothness. , A matting effect can be expected in the formulation.
Spherical particles made of plastic such as polystyrene, polyethylene, polypropylene, nylon, and acrylic are known as particles used in such a preparation.
これらプラスチックからなる球状粒子は、ファンデー
ション、パウダー類に用いられることが知られており、
単独で、もしくはこれに二酸化チタン、金属類の微粉末
等を付着せしめた複合原料として用いられることが多
く、その目的は、使用時の滑り、伸びの改善や、外界か
らの刺激より皮膚を保護し、製剤物性の改良に寄与する
ことにある。Spherical particles made of these plastics are known to be used in foundations and powders,
It is often used alone or as a composite raw material in which titanium dioxide, fine powders of metals, etc. are attached to it, and the purpose is to improve slippage and elongation during use and protect the skin from external stimuli. And contribute to the improvement of the physical properties of the preparation.
このように、洗浄剤、クリーム類、ファンデーション
等に使用される球状粒子は、製剤使用時の滑り、伸び等
の使用感の改善、摩擦によるマッサージ効果及び汚れの
除去等に有効であるとされていた。As described above, the spherical particles used for detergents, creams, foundations, etc. are said to be effective in improving the feeling of use such as slippage and elongation during use of the preparation, massage effect by friction, and removal of stains. It was
しかしながら、上記の球状粒子を配合した製剤中に生
薬抽出物をそのままの状態で添加した場合、生薬抽出物
中に含まれる成分によっては化粧品原料との反応や製剤
に対する溶解度の関係で、濁りや沈澱物を生じることが
あり、変色することも多い。さらに、精油成分や刺激性
成分が一時的に多量に付着すると、皮膚への悪影響とな
って現れる等好ましくない場合がある。However, when the crude drug extract is added as it is to the formulation containing the above spherical particles, depending on the components contained in the crude drug extract, it may become cloudy or precipitate depending on the reaction with cosmetic raw materials and the solubility in the formulation. It may cause discoloration and often discolor. Further, if a large amount of the essential oil component or the irritating component is temporarily adhered, it may have an adverse effect on the skin and may be undesirable.
本発明者らは、上記従来技術における球状粒子を配合
した生薬抽出物含有製剤の問題点を解決すべく研究し、
前記球状粒子として、微細孔を有する疎水性のスチレン
系吸着樹脂抽出物を使用し、これに生薬抽出物を吸着せ
しめる形態をとれば、上記従来技術における問題点がき
わめて良好に解決できることを見出し、この新しい発見
に基づいてさらに鋭意研究を重ねた結果本発明を完成す
るに到ったものである。The present inventors have studied to solve the problems of the herbal medicine extract-containing preparation containing the spherical particles in the above-mentioned conventional technology,
As the spherical particles, a hydrophobic styrene-based adsorption resin extract having fine pores is used, and if a form in which a crude drug extract is adsorbed to the spherical styrene-based adsorption resin extract, it is found that the problems in the above-mentioned conventional techniques can be solved very well, As a result of further intensive research based on this new discovery, the present invention has been completed.
すなわち、本発明は、微細孔を有する疎水性のスチレ
ン系吸着樹脂に生薬抽出物を吸着せしめたものを配合し
てなる粉体もしくは粒状体の化粧料である。That is, the present invention is a powdery or granular cosmetic comprising a mixture of a hydrophobic styrene-based adsorption resin having fine pores and a crude drug extract adsorbed thereto.
本発明で用いる微細孔を有する疎水性のスチレン系樹
脂は、一般的に知られている球形のプラスチック粒子と
はその機能において著しく異なるものである。The hydrophobic styrenic resin having fine pores used in the present invention is significantly different in function from the generally known spherical plastic particles.
すなわち、一般に球形のプラスチック粒子として知ら
れているものは、ナイロン、ポリエチレン、ポリスチレ
ン、架橋ポリスチレン等であるが、これら球形のプラス
チック粒子は吸着性がなく、生薬抽出物と配合すると単
に樹脂表面に生薬抽出物が付着する程度であり、プラス
チック粒子の中に吸蔵されることはない。このため、本
発明の目的とする生薬抽出物を徐々に粒子から放出し、
皮膚に対して生薬の持つ性能が徐々に発揮されるという
本発明の目的を達成することは出来ない。このことは、
プラスチック粒子の大きさを微小にしても変わらず、本
願発明の目的とする現象は得られない。That is, what is generally known as spherical plastic particles is nylon, polyethylene, polystyrene, cross-linked polystyrene, etc., but these spherical plastic particles do not have adsorptivity, and when blended with a crude drug extract, the crude drug is simply added to the resin surface. The extract is attached only and is not occluded in the plastic particles. Therefore, gradually release the crude drug extract targeted by the present invention from the particles,
It is not possible to achieve the object of the present invention that the performance of the crude drug is gradually exerted on the skin. This is
Even if the size of the plastic particles is made small, it does not change, and the phenomenon intended by the present invention cannot be obtained.
また、吸着樹脂としてはフェノール系やトリアジン環
を有するものもあるが、樹脂母体が親油性のものでは本
発明の化粧料に使用するスチレン系吸着樹脂のように特
異的な吸着性能を示さないので、このような樹脂も本発
明の目的を達成することができない。Further, as the adsorption resin, there are those having a phenolic or triazine ring, but if the resin matrix is lipophilic, it does not show a specific adsorption performance unlike the styrene-based adsorption resin used in the cosmetics of the present invention. However, such a resin cannot achieve the object of the present invention.
本発明で用いる疎水性のスチレン系吸着樹脂は、疎水
性の樹脂母体を有するスチレン系吸着樹脂であって、白
色、球状であり、耐薬品性に優れ、官能基を有せず、比
表面積が極めて大きく、物質により選択的に吸着性を有
する樹脂であり、その細孔径が140〜1,500nm、細孔容積
0.4〜15ml/g、比表面積400〜700m2/gのものが使用でき
る。The hydrophobic styrene-based adsorption resin used in the present invention is a styrene-based adsorption resin having a hydrophobic resin matrix, is white and spherical, has excellent chemical resistance, does not have a functional group, and has a specific surface area. It is a resin that is extremely large and selectively adsorbs depending on the substance. Its pore diameter is 140-1,500 nm, and pore volume.
0.4 to 15 ml / g and specific surface area of 400 to 700 m 2 / g can be used.
これを植物抽出液に加えると、一時的に植物抽出液を
吸着する。この植物抽出液を吸着した樹脂を乾燥するこ
とにより植物抽出液(植物抽出エキス)は、前記スチレ
ン系樹脂の中に固定化される。この植物抽出エキスを吸
着したスチレン系樹脂は、粉体、粒状体、固型製剤のい
ずれの製剤中に配合しても、植物抽出エキスが樹脂から
分離することはなく、安定な状態を保つことができる。
そして、これらの製剤を使用する場合、アルコール、多
価アルコールや溶剤類、界面活性剤、香料等を含有する
親油性物質を加えたり、水を加えて粉体、粒状体、固体
中の水溶性物質を溶解させ植物抽出エキスを含有した樹
脂と親油性物質を接触せしめることによって植物抽出エ
キスは樹脂から再び溶出し、製剤中に徐々に溶け込み、
使用部位に徐々に接触し、長時間低濃度で有効な状態を
保つ。また、前記スチレン系吸着樹脂は、皮膚表面から
取り除かれた汚れを吸着する性能も有し、洗浄補助剤と
しての効果も期待できる。When this is added to the plant extract, the plant extract is temporarily adsorbed. By drying the resin having adsorbed the plant extract, the plant extract (plant extract) is fixed in the styrene resin. The styrenic resin that has adsorbed the plant extract does not separate from the resin even if it is blended in any of powder, granule, and solid preparations, and keeps a stable state. You can
When using these preparations, lipophilic substances containing alcohols, polyhydric alcohols and solvents, surfactants, fragrances, etc. are added, or water is added to powders, granules, water-soluble substances in solids. By dissolving the substance and bringing the resin containing the plant extract into contact with the lipophilic substance, the plant extract elutes again from the resin and gradually dissolves in the formulation,
Keep in contact with the site of use gradually and maintain a low concentration for a long time to remain effective. Further, the styrene-based adsorbent resin also has a property of adsorbing dirt removed from the skin surface, and an effect as a cleaning aid can be expected.
本発明で用いられる生薬は、和漢生薬、西洋生薬、あ
るいは民間薬として用いられるものを含め、広い範囲の
ものを用いることができる。The crude drug used in the present invention can be used in a wide range including those used as Japanese and Chinese crude drugs, Western crude drugs, or folk medicine.
例えば山梔子、黄連、黄柏、人参、橙皮、陳皮、 大蒜、石菖、 紅花、牡丹皮、生姜、芍薬、沢潟、大棗、麦門冬、黄
耆、杏仁、桃仁、甘草、山査子、連翹、茴香、 苫参、桑白皮、地黄、当薬、営実、丁子、延命草、枇杷
葉、薄荷、地楡、金銀花、当帰、桃葉、虎耳草、山椒、
艾葉、荊芥、紫銀、松藤、車前草、車前子、厚朴、松、 防風、浜防風、エンジュ(槐)、アロエ、キャロット、
シラカバ、カミツレ、ヘンナ、アルニカ、トンキンセン
カ、リンドウ、ゼラニウム、ハマメリス、ホップ、アイ
リス、マヨナラ、セイヨウトチノキ、メリッサ、オトギ
リソウ、ミルラ、コケモモ、パパイヤ、サルビア、タチ
ジャコウソウ、トショウ、ボダイジュ、ジュニパー、タ
イム、ローズマリー、マツ、スギナ、ユーカリ、マロニ
エ、ショウブ、セイヨウノコギリソウ、セイヨウニワト
コ、セイヨウキズタ、セイヨウドリギ、メリーロート、
ローマカミツレ、ヤグルマギク、ノイバラ、その他に
茶、レモン、オレンジ、ライム、バラ、ラベンダー等、
芳香性の植物類の抽出物も用いることができ、これらの
植物の含有する親油性物質を主体に吸着させることがで
きる。For example, Yamajiko, Huanglian, Huangbai, carrot, orange peel, Chen skin, Large garlic, iris, Safflower, peony skin, ginger, peony, Sawagata, oju, bakumon winter, yellow 耆, apricot kernel, peach kernel, licorice, yamazushi, renja, scent, Tomato ginseng, mulberry bark, ground yellow, our medicine, Yomi, chopsticks, Enmeisou, loquat leaf, light load, ground bud, gold and silver flower, toki, peach leaf, tiger ear grass, Japanese pepper,
Abacus leaf, Peony, Purple silver, Matsufuji, Carmae grass, Carmaco, Hoboku, Matsu, Windbreak, beach windbreak, Enju (Maki), aloe, carrot,
White birch, chamomile, henna, arnica, ton calendula, gentian, geranium, hamamelis, hops, iris, mayonnara, horse chestnut, melissa, hypericum, myrrh, cowberry, papaya, salvia, adachi, juniper, juniper, juniper. Marie, pine, horsetail, eucalyptus, horse chestnut, ginger, yarrow, St. elderberry, St. John's wort, St.
Roman chamomile, cornflower, Neubara, other tea, lemon, orange, lime, rose, lavender, etc.
Extracts of aromatic plants can also be used, and lipophilic substances contained in these plants can be mainly adsorbed.
生薬抽出物の溶剤としてはアルコール類、多価アルコ
ール類の単独もしくは2種類以上の溶剤に水を配合して
なる混合溶剤が好ましく、更にこの混合した溶剤に対し
親油性物質や界面活性剤、香料、色素等を少量加えるこ
とが出来る。親油性物質としては化粧品原料として公知
の油脂類、ロウ類、炭化水素類、脂肪酸類、エステル類
等が適当であって、前記混合溶剤に分散、可溶化、乳化
した状態で使用することが出来る。The solvent for the crude drug extract is preferably an alcohol, a polyhydric alcohol, or a mixed solvent obtained by mixing two or more kinds of solvents with water, and a lipophilic substance, a surfactant, and a fragrance for the mixed solvent. A small amount of pigment, etc. can be added. As the lipophilic substance, fats, waxes, hydrocarbons, fatty acids, esters and the like which are known as raw materials for cosmetics are suitable, and can be used in a state of being dispersed, solubilized or emulsified in the mixed solvent. .
化粧料に利用される植物類は、一般に親油性や親水性
の溶剤によって抽出され、この抽出液を化粧品製剤に添
加して使用している。これらの抽出液は、多種の成分を
含有していることや、各種の原料の中に混合されること
によって他の成分からの影響を受けやすくなり、変色し
たり、沈澱物を生じたり、異臭を放ったり、外観上の変
化だけでなく有効成分の変化も受けやすく、また、有効
成分とともに悪臭の原因物質も同時に抽出するため香り
が悪く、利用できないこともある。The plants used for cosmetics are generally extracted with a lipophilic or hydrophilic solvent, and this extract is added to a cosmetic preparation for use. These extracts contain various components and are easily affected by other components when mixed in various raw materials, causing discoloration, formation of precipitates, and offensive odor. It is not easy to use because it is apt to be subject to changes in the active ingredients as well as changes in appearance, and because the causative agent of the malodor is extracted at the same time as the active ingredients, the scent is bad.
本発明で使用するスチレン系吸着樹脂は、有効成分と
ともに悪臭成分も吸着するため、悪臭物質の香りを弱
め、有効成分の香りの強さを適当に調節することもでき
る。その結果、従来、有効成分は利用したいがその悪臭
に問題のあった植物を化粧料に利用することができるよ
うになり、この点も本発明の大きな利点である。Since the styrenic adsorption resin used in the present invention adsorbs the malodorous component as well as the active ingredient, the odor of the malodorous substance can be weakened and the intensity of the odor of the active ingredient can be appropriately adjusted. As a result, it becomes possible to utilize a plant which has conventionally been required to use an active ingredient but has a problem of its bad odor in cosmetics, which is also a great advantage of the present invention.
生薬中の油溶生物質から水溶性物質までの広い範囲の
成分を抽出しやすくする為に、エタノールと水の混液
(エタノール40〜90%)を通常よく用いている。この溶
剤100部に対し、5部〜50部の生薬を浸漬し、抽出後濾
過して得られる生薬抽出液はガラスピンに密封して保存
すると、早くて3日、遅いものでも6ヶ月で浮遊物や沈
澱物などの異物の発生が認められ、異臭を発生したり色
調に変化の見られるものも多く、常温で安定に保つこと
が困難である。このことは、前述の生薬の殆どのものに
ついて言えることであり、更に製剤の目的に必要な要素
として数種類の生薬を配合することは、一層成分が多種
になり、安定性を欠き、一定の品質のものを得ることが
できないので、2種以上の生薬を同時に混合抽出するこ
とは極めて困難であった。A mixture of ethanol and water (40-90% ethanol) is often used to facilitate the extraction of a wide range of components from crude oils to water-soluble substances in crude drugs. 5 to 50 parts of crude drug is soaked in 100 parts of this solvent, and the crude drug extract obtained by filtering after extraction is stored in a glass pin sealed and stored. It is difficult to keep it stable at room temperature because many foreign substances such as substances and precipitates are recognized, and there are many cases that an offensive odor is generated or the color tone is changed. This can be said for most of the above-mentioned crude drugs, and further compounding several types of crude drugs as necessary elements for the purpose of the formulation makes the ingredients more diverse, lacks stability, and has a certain quality. Therefore, it was extremely difficult to simultaneously extract two or more crude drugs by mixing and extracting them.
本発明によれば、生薬抽出液に前記スチレン系吸着樹
脂を加えることにより、生薬の成分を選択的に吸着する
ことができ、成分同士の接触を少なくし、2種以上の生
薬でも個々にスチレン系吸着樹脂に吸着させた後配合す
れば、お互いの成分の反応を起こすことなく、長期間製
剤中で安定に保つことができる。According to the present invention, by adding the styrene-based adsorption resin to the crude drug extract, the components of the crude drug can be selectively adsorbed, the contact between the components is reduced, and even if two or more kinds of crude drugs are individually styrene-containing. If they are mixed after being adsorbed on the system-adsorbing resin, they can be kept stable in the formulation for a long period of time without causing mutual reaction of the components.
更に、前記スチレン系吸着樹脂に吸着された生薬成分
は、同時に吸着されたエターノル及び水が加熱乾燥され
ることによって除去されるので、2種以上の生薬の成分
同士の接触も少なく、しかも油溶性の溶剤を含んだ製剤
中にスチレン系吸着樹脂をくわえると、生薬の有効成分
を徐々に溶出し、生薬抽出液を添加して得た製剤と同様
の目的を得るように調節することもできる。Furthermore, since the herbal drug components adsorbed on the styrene-based adsorbent resin are removed by heating and drying the adsorbed ethanol and water at the same time, there is little contact between two or more herbal drug components, and the oil solubility is low. When a styrene-based adsorbent resin is added to the preparation containing the above solvent, the active ingredient of the crude drug can be gradually eluted, and it can be adjusted to obtain the same purpose as the preparation obtained by adding the crude drug extract.
本発明に用いるスチレン系吸着樹脂に生薬抽出液を吸
着せしめるには、前記スチレン系吸着樹脂1に対し、生
薬抽出物を2〜3の比率で含浸させ、室温または加温条
件下で24時間乾燥する。このようにして得られたスチレ
ン系吸着樹脂は、そのままの状態または被覆形成物で被
覆させた後、これに粉体原料を加えて粒状にするか、あ
らかじめ粒状化した化粧品原料に生薬抽出物を含有した
スチレン系吸着樹脂を配合して目的とする化粧料を製す
ることができる。In order to allow the crude drug extract to be adsorbed on the styrene-based adsorption resin used in the present invention, the crude drug extract is impregnated in the styrene-based adsorption resin 1 at a ratio of 2 to 3 and dried at room temperature or under heating conditions for 24 hours. To do. The styrene-based adsorption resin thus obtained is in the state as it is or after being coated with a coating-forming material, and then powdered raw material is added thereto to form granules, or a crude drug extract is added to a pre-granulated cosmetic raw material. A desired cosmetic can be produced by blending the contained styrene-based adsorption resin.
次に、本発明による生薬抽出物を吸着せしめたスチレ
ン系吸着樹脂を配合した化粧料の皮膚刺激が緩和である
ことを示すために、人体の皮膚に対する影響を試験した
ので、以下に記載する。Next, in order to show that the skin irritation of the cosmetic containing the styrene-based adsorbent resin adsorbing the crude drug extract according to the present invention was mild, the effect on human skin was tested, and is described below.
(試料の調製) に対し、イソプロピルアルコール10%、エチルアルコー
ル70%、精製水20%からなる溶剤10部を加え、24時間室
温にて放置後、濾過して を得る。この を1時間40℃に加温してアルコールの大半を除去し、こ
れを白色ワセリン10部に加え練り込んで試料Aとする。(Preparation of sample) To 10 parts of isopropyl alcohol, 70% of ethyl alcohol, and 20% of purified water were added, and the mixture was allowed to stand at room temperature for 24 hours and then filtered. Get. this Is heated to 40 ° C. for 1 hour to remove most of the alcohol, and this is added to 10 parts of white petrolatum and kneaded to obtain a sample A.
一方、 にスチレン系吸着樹脂1部を加えて30分間撹拌すると、
液は無色となり、 を吸着した樹脂が下層に沈降する。この樹脂を50℃で2
時間乾燥して得たスチレン系吸着樹脂1部を白色ワセリ
ン10部に加え練り合わせて試料Bとする。on the other hand, Add 1 part of styrene-based adsorption resin to and stir for 30 minutes,
The liquid becomes colorless, The resin that has adsorbed is settled in the lower layer. 2 this resin at 50 ℃
1 part of a styrene-based adsorption resin obtained by drying for an hour is added to 10 parts of white petrolatum and kneaded to obtain a sample B.
以上のようにして得た試料Aと試料Bとをそれぞれ健
康な男女15名を対象に、各々直径20mmの円形状に前腕屈
側に塗り、そのままの状態で24時間経過後、かゆみ、痛
み、発赤の発生を調べたところ、次の結果が得られた。The samples A and B obtained as described above were applied to 15 healthy men and women, respectively, in a circular shape with a diameter of 20 mm, applied to the flexion side of the forearm, and after 24 hours, the itch, pain, When the occurrence of redness was examined, the following results were obtained.
試料Aでは23%の人がかゆみ若しくは痛みを伴う発赤
が認められたのに対し、かゆみ、痛みを感じないで発赤
を認められた人が67%あった。試料Bでは17%弱の人が
発赤を認めたものの、かゆみや痛みは伴わず、本発明に
よる化粧料の皮膚刺激が緩和であることが証明された。 In sample A, 23% of people had itching or painful redness, while 67% had redness without feeling itching or pain. In sample B, a little less than 17% of people recognized redness, but itching and pain were not accompanied, and it was proved that the skin irritation of the cosmetic according to the present invention was mild.
次に、実施例を以て本発明を更に詳しく説明するが、
本発明は、これら実施例により限定されるものではな
い。Next, the present invention will be described in more detail with reference to Examples.
The present invention is not limited to these examples.
実施例1 粉末状パック 山梔子5部(部は重量部を示す。以下実施例において
同じ)に対し、プロピレングリコール10%、グリセリン
5%、エチルアルコール70%、精製水15%からなる溶剤
15部を加え、24時間室温にて放置後、濾過して茶褐色の
抽出液を得て山梔子抽出液Bとする。この山梔子抽出液
B3部にスチレン系吸着樹脂デュオライトS−861(商品
名,住友化学工業株式会社製)2部を加え30分間撹拌す
ると、抽出液下層に山梔子エキスを吸着した樹脂が沈降
する。この樹脂を50℃で2時間加熱乾燥して山梔子エキ
ス吸着樹脂を得る。Example 1 A solvent composed of 10% propylene glycol, 5% glycerin, 70% ethyl alcohol, and 15% purified water with respect to 5 parts of powdered pack Yamajiko (parts represent parts by weight; the same applies to the following examples).
After adding 15 parts and allowing it to stand at room temperature for 24 hours, it is filtered to obtain a brownish brown extract, which is referred to as Yamabushi extract B. This Yamajiko extract
When 2 parts of styrene-based adsorption resin Duolite S-861 (trade name, manufactured by Sumitomo Chemical Co., Ltd.) is added to 3 parts of B3 and stirred for 30 minutes, the resin which adsorbed the Yamajiko extract is precipitated in the lower layer of the extract. This resin is heated and dried at 50 ° C. for 2 hours to obtain a Yamajiko extract adsorption resin.
次にこの山梔子エキス吸着樹脂1〜20部を下記の原料
からなる粉末状パック組成物80〜99部に加え、万能混合
撹拌機(三英製作所製)で30分間均一に撹拌混合して粉
末状パック2kgを製する。Next, add 1 to 20 parts of this Yamajiko extract adsorbent resin to 80 to 99 parts of a powdered pack composition made of the following raw materials, and stir and mix them uniformly for 30 minutes with a universal mixing stirrer (manufactured by Sanei Seisakusho). Produces 2 kg of packs.
クレー 50% タルク 20% 酸化亜鉛 10% 二酸化チタン 5% ホホバ油 1% モノラウリン酸 3% ポリオキシエチレンソルビタングリセリン 10% 無水ケイ酸 適量 香料 適量 このようにして得た粉末状パック1〜2gを、化粧水、
乳液、水などでよく練り、ペースト状として皮膚に塗布
し、乾くまで放置後、水または湯で洗い流す。Clay 50% Talc 20% Zinc oxide 10% Titanium dioxide 5% Jojoba oil 1% Monolauric acid 3% Polyoxyethylene sorbitan glycerin 10% Silicic acid An appropriate amount Perfume An appropriate amount water,
Thoroughly knead with an emulsion or water, apply as a paste to the skin, leave to dry, then rinse with water or hot water.
実施例2 粒状洗顔剤 当帰10部に対しポリエチレングリコール600 10%、エ
チルアルコール70%、精製水20%からなる溶剤10部を加
え、24時間室温にて放置後、濾過して淡黄色の抽出液を
得て当帰抽出液Bとする。この当帰抽出液B3部にスチレ
ン系吸着樹脂デュオライトS−861(商品名,住友化学
工業株式会社製)1部を加え30分間撹拌すると、抽出液
下層に当帰エキスを吸着した樹脂が沈降する。この樹脂
を50℃、2時間で乾燥し、本発明品である当帰エキス吸
着樹脂を得る。Example 2 Granular face cleansing agent To 10 parts by weight, 10 parts of a solvent consisting of 10% polyethylene glycol 600, 70% ethyl alcohol and 20% purified water was added, and the mixture was allowed to stand at room temperature for 24 hours and then filtered to obtain a pale yellow extract. The liquid is obtained and designated as Toki Extract B. 1 part of styrene-based adsorption resin Duolite S-861 (trade name, manufactured by Sumitomo Chemical Co., Ltd.) was added to 3 parts of this Toki extract B, and the mixture was stirred for 30 minutes. To do. This resin is dried at 50 ° C. for 2 hours to obtain the Toki extract adsorption resin which is the product of the present invention.
次にラウリル硫酸ナトリウム10部、ラウロイルサルコ
シンナトリウム10部、Nラウロイルメチルタウリンナト
リウム10部、ソルビトール1.0部、タルク20部、クレー1
0部、無水ケイ酸適量、に少量のスクワランを加えよく
混和し、適量の水を加えて撹拌混和後、押出し造粒機に
かけた後乾燥し、整粒して粒状洗顔剤基剤を得る。Next, sodium lauryl sulfate 10 parts, lauroyl sarcosine sodium 10 parts, N-lauroylmethyl taurine sodium 10 parts, sorbitol 1.0 part, talc 20 parts, clay 1
A small amount of squalane is added to 0 part of silicic acid anhydride and mixed well, an appropriate amount of water is added and mixed by stirring, and then the mixture is subjected to extrusion granulation, dried and sized to obtain a granular facial cleansing agent base.
本実施例では洗顔剤基剤を押出し造粒法である湿式造
粒法の一例として記載したが、造粒法はこれに限定する
のではなく、他の方法、例えば破砕造粒法、転動造粒
法、流動層造粒法等を適宜選択することができる。In this example, the facial cleansing agent base was described as an example of the wet granulation method which is an extrusion granulation method, but the granulation method is not limited to this, and other methods such as a crushing granulation method and rolling A granulation method, a fluidized bed granulation method or the like can be appropriately selected.
本発明による造粒洗顔剤は上記の当帰エキス吸着樹脂
1〜20部を粒状洗顔剤基剤80〜99部に加え、混合して粒
状洗顔剤2kgを製する。このようにして得た粒状洗顔剤
4〜5gに水を加えて練り、ペースト状として洗顔し、水
で洗い流す。The granulated face cleansing agent according to the present invention is prepared by adding 1 to 20 parts of the above-mentioned Toki extract adsorption resin to 80 to 99 parts of the granular facial cleansing agent base and mixing them to prepare 2 kg of the granular facial cleansing agent. Water is added to 4 to 5 g of the thus obtained granular facial cleanser, and the mixture is kneaded to form a paste, which is washed with water and rinsed with water.
上記のように、本発明の化粧料は、微細孔を有する疎
水性のスチレン系吸着樹脂に生薬抽出物を吸着せしめた
ものを配合してなる粉体もしくは粒状体の化粧料である
から、微細な多孔質の球状粒子の内部に吸蔵せしめられ
た生薬抽出物は、この球状粒子を化粧料製剤中に混入し
た場合も製剤中に生薬抽出物を溶出させることなく安定
に保たれ、使用時皮膚表面の温度及び油溶性成分、水分
によって生薬抽出物が徐々にスチレン系吸着樹脂から溶
出して皮膚に対し生薬のもつ性能が徐々に発揮され、し
かも、必要なだけの量が溶出して皮膚に接触するので皮
膚に対する炎症等の弊害もなく、生薬のもつ性能が徐々
に発揮されるという、種々の優れた効果を奏するもので
ある。As described above, the cosmetic of the present invention is a powdery or granular cosmetic containing a mixture of a hydrophobic styrene-based adsorption resin having fine pores and a crude drug extract adsorbed thereon. The herbal medicine extract stored in the inside of such porous spherical particles is kept stable without eluting the herbal medicine extract in the formulation even when these spherical particles are mixed in the cosmetic preparation, and the skin is not used during use. The crude drug extract gradually elutes from the styrene-based adsorption resin due to surface temperature, oil-soluble components, and water, and the performance of the crude drug is gradually exerted on the skin, and the necessary amount elutes on the skin. Since they come into contact with each other, there is no adverse effect such as inflammation on the skin, and the performance of the herbal medicine is gradually exhibited, thus exhibiting various excellent effects.
Claims (2)
脂に生薬抽出物を吸着せしめたものを配合してなる粉体
もしくは粒状体の化粧料。1. A powdery or granular cosmetic comprising a mixture of a hydrophobic styrene-based adsorption resin having fine pores and a crude drug extract adsorbed thereto.
00nm、細孔容積0.4〜1.5ml/g、比表面積400〜700m2/gの
スチレン系吸着樹脂であることを特徴とする特許請求の
範囲第1項の粉体もしくは粒状体の化粧料。2. A styrene-based adsorption resin having a pore size of 140 to 1,5
The powdery or granular cosmetic material according to claim 1, which is a styrene-based adsorption resin having 00 nm, a pore volume of 0.4 to 1.5 ml / g, and a specific surface area of 400 to 700 m 2 / g.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62192656A JP2504064B2 (en) | 1987-08-03 | 1987-08-03 | Cosmetics |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62192656A JP2504064B2 (en) | 1987-08-03 | 1987-08-03 | Cosmetics |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6438008A JPS6438008A (en) | 1989-02-08 |
| JP2504064B2 true JP2504064B2 (en) | 1996-06-05 |
Family
ID=16294863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62192656A Expired - Lifetime JP2504064B2 (en) | 1987-08-03 | 1987-08-03 | Cosmetics |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2504064B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102061613B1 (en) | 2019-05-24 | 2020-01-02 | 비비솔루션 주식회사 | Manufacturing method of cosmetic composition having deodorization and antimicrobial effect using microcapsule adsorbed with asarum oil and cosmetic composition including the same |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3586519B2 (en) * | 1996-08-02 | 2004-11-10 | 株式会社ノエビア | Antibacterial hypoallergenic cosmetics |
| JP4896557B2 (en) * | 2006-03-29 | 2012-03-14 | 株式会社コーセー | Gommage cosmetic |
-
1987
- 1987-08-03 JP JP62192656A patent/JP2504064B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102061613B1 (en) | 2019-05-24 | 2020-01-02 | 비비솔루션 주식회사 | Manufacturing method of cosmetic composition having deodorization and antimicrobial effect using microcapsule adsorbed with asarum oil and cosmetic composition including the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6438008A (en) | 1989-02-08 |
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