JPH036180B2 - - Google Patents

Info

Publication number
JPH036180B2
JPH036180B2 JP28493085A JP28493085A JPH036180B2 JP H036180 B2 JPH036180 B2 JP H036180B2 JP 28493085 A JP28493085 A JP 28493085A JP 28493085 A JP28493085 A JP 28493085A JP H036180 B2 JPH036180 B2 JP H036180B2
Authority
JP
Japan
Prior art keywords
parts
weight
fatty acid
composition
gel
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
Application number
JP28493085A
Other languages
Japanese (ja)
Other versions
JPS62143971A (en
Inventor
Shigeru Mori
Satoshi Kuwata
Koji Sakuta
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP28493085A priority Critical patent/JPS62143971A/en
Publication of JPS62143971A publication Critical patent/JPS62143971A/en
Publication of JPH036180B2 publication Critical patent/JPH036180B2/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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • 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
    • 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
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野〕 本発明はゲル状組成物、特にはシリカなどの充
填剤を使用しない、化粧品用基材などに有用とさ
れるシリコーンオイルを主材とするゲル状組成物
に関するものである。 (従来の技術) 化粧品用、医療用のペースト、クリーム、プレ
ス状組成物などには各種のシリコーンオイルが添
加配合されているが、シリコーン組成物を基材と
する利用例は少ない。 これはシリコオーオイルをゲル状物とするには
無機質充填剤としての疎水性シリカ、ベントンな
どの増粘剤の添加が必要であり、使用するシリコ
ーオイルも25℃における粘度が100cS以上である
比較的高粘度のものとする必要があるために、こ
のようにして得られたゲル状物を皮膚表面に塗布
した場合には伸度感が重く、また揮発分が殆んど
ないのでべたつき感が長期にわたつて残留する不
利があるからとされている。 したがつて、これらの欠点を解決した低粘度で
揮発性に富むシリコーンを主剤とするゲル状組成
物が待望されている。 (発明の構成) 本発明は上記したような不利を解決したシリコ
ーン系のゲル状組成物に関するものであり。これ
は、(1)式 示される環状ジメチルポリシロキサン30〜90重量
部、(2)炭素数8〜24の脂肪酸と炭素数1〜24の脂
肪酸アルコールとのエステルまたは炭素数10〜40
の脂肪族炭化水素から選択される1種または2種
以上の混合物5〜50重量部、(3)デキストリン脂肪
酸エステル5〜30重量部とからなることを特徴と
するものである。 すなわち、本発明者らは等に化粧品用、医療用
などに有用とされるシリコーンオイルを主剤とす
るゲル状組成物について種々検討した結果、シリ
コーンオイルとして上記した式で示される環状ジ
メチルポリシロキサンを使用すると共に、このゲ
ル化剤として高級脂肪酸の脂肪族アルコールとの
エステルまたは脂肪族炭化水素とデキストリン脂
肪酸エステルを使用すると所期のゲル状組成物が
容易に得られ、このゲル状組成物はこれを皮膚な
どに塗布した場合に進展性が軽快で使用感もさつ
ぱりしており、塗布後は環状ジメチルポリシロキ
サンが蒸発するために濡れ感覚が何時までも残る
ことがないということを確認して本発明を完成さ
せた。 本発明のゲル状組成物を構成する第1成分とし
てのシリコーンオイルは、式 で示される環状ジメチルポリシロキサンとされる
が、このものはこれを含有するゲル状組成物を使
用後に発揮するものであることが望ましいので、
このn値は3〜6のものとされる。なお、このも
のは1種の使用でもよく、2種以上の混合物であ
つてもよいが、この使用量はゲル状組成物100重
量部におけるこの第1成分の量が30重量部以下で
は他成分が多くなりすぎて本組成物に期待される
軽快な進展性を乏しくなるし、べたつき感も増大
し、90重量部以上とすると十分なゲル化に至れな
くなるので、30〜90重量部の範囲とすることが必
要とされるが、この好ましい範囲は40〜8重量部
とされる。 また、この組成物における第2成分は前記した
ように炭素数が8〜20の高級脂肪酸と炭素数1〜
24の脂肪族アルコールとのエステルまたは炭素数
10〜40の脂肪族炭化水素とされ、これについては
ミリスチン酸イソプロピル、ミリスチン酸ブチ
ル、ミリスチン酸ミリスチル、ミリスチン酸オク
チルデシル、イソオクチル酸セチル、オレイル酸
デシル、ステアリン酸ブチル、ラウリン酸ヘキシ
ル、パルミチン酸イソプロピル、パルミチン酸ブ
チルなどの高級脂肪酸モノエステル、ジオレイン
酸プロピレングリコール、ジ−2−エチルヘキサ
ン酸ネオペンチルグリコールなどの高級脂肪酸ジ
エステル、カプリル酸トリグリセリド、カプリン
酸トリグリセリドなどの高級脂肪酸トリエステル
など、さらにはスクワラン、アイソパー〔エクソ
ン化学(株)製、脂肪族炭化水素系溶剤の商品名〕な
どが例示されるが、これらはその1種で使用して
も2種以上の混合物であつてもよい。なお、この
第2成分の使用量はゲル化組成物100重量部中に
おけるこの成2成分の量が5重量部以下では第1
成分としてのシリコーンオイルがゲル化するまで
には至らず、50重量部以上とすると得られるゲル
状組成物が軽快な伸展性の乏しいものとなり、べ
たつき感も増大するので5〜50重量部の範囲とす
る必要があるが、この好ましい範囲は7〜45重量
部とされる。 つぎにこのゲル状組成物における第3成分とし
てのデキストリン脂肪酸エステルは例えば構造式
が次式 で示され、Aは水素原子または炭素数8〜20のの
アシル基で全Aモル数の50%以上はアシル基、l
は20〜30とされるものであり、この使用量はゲル
状組成物100重量部中におけるこの第3成分の量
が5重量部以下ではシリコールオイルのゲル化が
進まず、30重部以上とすると得られる組成物が固
くなりすぎて伸展性の乏しいものとなるので5〜
30重量部の範囲とするることが必要とされるが、
この好ましい範囲は7〜25重量部とされる。 本発明のゲル状組成物は上記した第1成分〜第
3成分の所定量を均一に混合することによつて得
ることができるが、この混合は50〜100℃で行う
ことがよく、例えば100℃以下で加温撹拌も行つ
て前記した脂肪酸エステルまたは脂肪族炭化水素
およびデキストリン樹脂エステルをシリコーンオ
イルに均一に溶解してから冷却すれば目的とする
均質なゲル状組成物を得ることができる。なお、
この組成物に各種の油性剤、香料、医薬用成分、
酸化防止剤、顔料、染料などを添加することは本
発明の組成物の特性に大きな変更を来たさない範
囲であれば任意とされる。 つぎに本発明の実施例をあげるが、例中の部は
重量部を、また粘度は25℃での測定値を示したも
のである。 実施例 1〜10 第1表に示した量のオクタメチルシクロテトラ
シロキサン・KF994(信越化学工業(株)製商品名〕
およびデカメチルシクロペンタシロキサンKF995
〔同社製商品名〕に第1表に示した種類および量
の高級脂肪酸エステルまたは脂肪族炭化水素なら
びに第1表に示した量のデキストリン脂肪酸エス
テル・レオパールKL〔千葉製粉(株)製商品名〕を添
加し、この総量300gを500mlの硬質ガラスフラス
コ中に投入し、60〜70℃で撹拌して均一溶液とな
つたことを確認して撹拌を停止し、氷水浴で急冷
したところ、均一なゲル状組成物が得られたの
で、この組成物についての稠度、離油度をJIS
K2220に準拠した方法で測定したところ第1表に
併記したとうりの結果が得られた。
(Industrial Application Field) The present invention relates to a gel composition, particularly a gel composition based on silicone oil that does not use fillers such as silica and is useful as a base material for cosmetics. (Prior art) Various silicone oils are added to pastes, creams, pressed compositions, etc. for cosmetics and medical purposes, but there are few examples of use of silicone compositions as a base material. To make silico-oil into a gel, it is necessary to add thickeners such as hydrophobic silica and bentone as inorganic fillers, and the silico-oil used also has a viscosity of 100 cS or more at 25°C. Because it needs to have a high viscosity, when the gel-like material obtained in this way is applied to the skin surface, it feels heavy and has a long-lasting sticky feeling because it has almost no volatile content. Accordingly, there has been a long-awaited need for a gel-like composition based on silicone, which has low viscosity and high volatility and solves these drawbacks. (Structure of the Invention ) The present invention relates to a silicone-based gel composition that solves the above-mentioned disadvantages. 30 to 90 parts by weight of the indicated cyclic dimethyl polysiloxane, (2) an ester of a fatty acid having 8 to 24 carbon atoms and a fatty acid alcohol having 1 to 24 carbon atoms or 10 to 40 carbon atoms;
(3) dextrin fatty acid ester (5 to 30 parts by weight). That is, as a result of various studies conducted by the present inventors on gel compositions based on silicone oil, which are useful for cosmetics, medical applications, etc., we have found that cyclic dimethylpolysiloxane represented by the above formula is used as the silicone oil. In addition, if an ester of a higher fatty acid with an aliphatic alcohol or an aliphatic hydrocarbon and a dextrin fatty acid ester is used as the gelling agent, the desired gel composition can be easily obtained. We have confirmed that when applied to the skin, the spread is light and the feeling is refreshing, and the cyclic dimethylpolysiloxane evaporates after application, so the wet feeling does not remain for any length of time. The present invention was completed. The silicone oil as the first component constituting the gel composition of the present invention has the formula It is said to be a cyclic dimethylpolysiloxane represented by, but it is desirable that this product exhibits its properties after using a gel composition containing it.
This n value is set to 3 to 6. Note that this substance may be used alone or in a mixture of two or more types, but if the amount of this first component is 30 parts by weight or less in 100 parts by weight of the gel composition, other components may be used. If the amount exceeds 90 parts by weight, it will impair the easy spreadability expected of this composition, increase the stickiness, and if it exceeds 90 parts by weight, sufficient gelation will not be achieved. The preferred range is 40 to 8 parts by weight. Further, as described above, the second component in this composition is a higher fatty acid having 8 to 20 carbon atoms and a higher fatty acid having 1 to 20 carbon atoms.
Esters with aliphatic alcohols of 24 or carbon numbers
10 to 40 aliphatic hydrocarbons, including isopropyl myristate, butyl myristate, myristyl myristate, octyldecyl myristate, cetyl isooctylate, decyl oleate, butyl stearate, hexyl laurate, and isopropyl palmitate. , higher fatty acid monoesters such as butyl palmitate, higher fatty acid diesters such as propylene glycol dioleate, neopentyl glycol di-2-ethylhexanoate, higher fatty acid triesters such as caprylic acid triglyceride and capric acid triglyceride, and even squalane. , Isopar [manufactured by Exxon Chemical Co., Ltd., trade name of aliphatic hydrocarbon solvent], etc., and these may be used alone or in a mixture of two or more. Note that if the amount of this second component used is 5 parts by weight or less in 100 parts by weight of the gelling composition, the amount of the second component used is less than the first amount.
If the silicone oil as a component does not gel, and if it exceeds 50 parts by weight, the resulting gel-like composition will have poor light extensibility and increase stickiness, so use a range of 5 to 50 parts by weight. The preferred range is 7 to 45 parts by weight. Next, the dextrin fatty acid ester as the third component in this gel composition has, for example, the following structural formula: A is a hydrogen atom or an acyl group having 8 to 20 carbon atoms, and 50% or more of the total number of moles of A is an acyl group, l
is said to be 20 to 30, and if the amount of this third component is less than 5 parts by weight in 100 parts by weight of the gel composition, gelation of the silicone oil will not proceed; If this is done, the resulting composition will be too hard and have poor extensibility, so
A range of 30 parts by weight is required, but
The preferred range is 7 to 25 parts by weight. The gel composition of the present invention can be obtained by uniformly mixing predetermined amounts of the first to third components described above, but this mixing is preferably carried out at 50 to 100°C, for example at 100°C. The desired homogeneous gel composition can be obtained by uniformly dissolving the aforementioned fatty acid ester or aliphatic hydrocarbon and dextrin resin ester in silicone oil by heating and stirring at a temperature below .degree. C. and then cooling. In addition,
This composition includes various oily agents, fragrances, pharmaceutical ingredients,
Addition of antioxidants, pigments, dyes, etc. is optional as long as it does not significantly change the properties of the composition of the present invention. Next, examples of the present invention will be given, in which parts are parts by weight, and viscosity is a value measured at 25°C. Examples 1 to 10 Octamethylcyclotetrasiloxane KF994 (trade name manufactured by Shin-Etsu Chemical Co., Ltd.) in the amounts shown in Table 1
and decamethylcyclopentasiloxane KF995
[Product name manufactured by the company] higher fatty acid ester or aliphatic hydrocarbon of the type and amount shown in Table 1 and dextrin fatty acid ester Leopard KL in the amount shown in Table 1 [Product name manufactured by Chiba Flour Milling Co., Ltd.] The total amount of 300g was put into a 500ml hard glass flask, stirred at 60 to 70℃, and after confirming that it had become a homogeneous solution, stirring was stopped and quenched in an ice water bath. Since a gel-like composition was obtained, the consistency and oil separation degree of this composition were determined by JIS.
When measured using a method based on K2220, the results shown in Table 1 were obtained.

【表】 比較例 実施例で使用した環状ジメチルポリシロキサ
ン・KF994またはKF995 270部に、デキストリン
脂肪エステル・レオパールKL〔千葉製粉(株)製商品
名〕30部を添加し、500mlの硬化ガラスフラスコ
中で60〜70℃に撹拌したが、レオパールKLはシ
リコーンオイルに均一に溶解せず、撹拌後に氷水
浴で急冷したものはレオパールKLが沈殿となり、
全くゲル化は認められなかつた。
[Table] Comparative Example To 270 parts of the cyclic dimethylpolysiloxane KF994 or KF995 used in the example, 30 parts of dextrin fatty ester Leopard KL [trade name manufactured by Chiba Flour Milling Co., Ltd.] was added, and the mixture was placed in a 500 ml hardened glass flask. Although the mixture was stirred at 60 to 70℃, Leopard KL did not dissolve uniformly in the silicone oil, and when it was rapidly cooled in an ice water bath after stirring, Leopard KL precipitated.
No gelation was observed at all.

Claims (1)

【特許請求の範囲】 1 (1) 式 で示される環状ジメチルポリシロキサン
30〜90重量部、 (2) 炭素数8〜24の脂肪酸と炭素数1〜24脂肪族
アルコールとのエステルまたは炭素数10〜40の
脂肪族炭化水素から選ばれる1種または2種以
上の混合物 5〜50重量部、 (3) デキストリン脂肪酸エステル 5〜30重量部 とからなることを特徴とするゲル状組成物。
[Claims] 1 (1) Formula Cyclic dimethylpolysiloxane represented by
30 to 90 parts by weight, (2) One or more mixtures selected from esters of fatty acids with 8 to 24 carbon atoms and aliphatic alcohols with 1 to 24 carbon atoms, or aliphatic hydrocarbons with 10 to 40 carbon atoms. (3) 5 to 30 parts by weight of dextrin fatty acid ester.
JP28493085A 1985-12-17 1985-12-17 Gelatinous composition Granted JPS62143971A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28493085A JPS62143971A (en) 1985-12-17 1985-12-17 Gelatinous composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28493085A JPS62143971A (en) 1985-12-17 1985-12-17 Gelatinous composition

Publications (2)

Publication Number Publication Date
JPS62143971A JPS62143971A (en) 1987-06-27
JPH036180B2 true JPH036180B2 (en) 1991-01-29

Family

ID=17684897

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28493085A Granted JPS62143971A (en) 1985-12-17 1985-12-17 Gelatinous composition

Country Status (1)

Country Link
JP (1) JPS62143971A (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH072631B2 (en) * 1987-03-06 1995-01-18 テルモ株式会社 Gel composition
JP2887485B2 (en) * 1989-08-09 1999-04-26 花王株式会社 Oily cosmetics
JP2631772B2 (en) * 1991-02-27 1997-07-16 信越化学工業株式会社 Novel silicone polymer and paste-like silicone composition having water dispersibility using the same
US5919437A (en) * 1996-05-24 1999-07-06 Colgate-Palmolive Company Cosmetic cream composition containing silicone gel material
JP4688291B2 (en) * 2000-12-28 2011-05-25 株式会社コーセー Oil makeup cosmetics
EP1935924B1 (en) 2002-09-12 2012-06-06 Shin-Etsu Chemical Company, Ltd. Pasty composition, and cosmetic preparation containing the same
JP6215719B2 (en) 2014-01-23 2017-10-18 信越化学工業株式会社 Cosmetics
JP6432244B2 (en) * 2014-09-24 2018-12-05 富士ゼロックス株式会社 Electrophotographic photosensitive member, process cartridge, and image forming apparatus
JP6285381B2 (en) 2015-03-13 2018-02-28 信越化学工業株式会社 Gel paste composition and cosmetics using the gel paste composition
JP2023057598A (en) 2021-10-12 2023-04-24 信越化学工業株式会社 Organoalkoxysilane-containing composition and production method of the same, and water absorption-preventive agent

Also Published As

Publication number Publication date
JPS62143971A (en) 1987-06-27

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