JP2849437B2 - Emulsified cosmetics and quasi-drugs - Google Patents

Emulsified cosmetics and quasi-drugs

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Publication number
JP2849437B2
JP2849437B2 JP2080996A JP8099690A JP2849437B2 JP 2849437 B2 JP2849437 B2 JP 2849437B2 JP 2080996 A JP2080996 A JP 2080996A JP 8099690 A JP8099690 A JP 8099690A JP 2849437 B2 JP2849437 B2 JP 2849437B2
Authority
JP
Japan
Prior art keywords
capsule
aqueous solution
storage chamber
solution component
component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2080996A
Other languages
Japanese (ja)
Other versions
JPH03284607A (en
Inventor
義治 坂東
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.)
Toyo Kasei Co Ltd
Original Assignee
Toyo Kasei 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 Toyo Kasei Co Ltd filed Critical Toyo Kasei Co Ltd
Priority to JP2080996A priority Critical patent/JP2849437B2/en
Priority to FR9103772A priority patent/FR2660212A1/en
Publication of JPH03284607A publication Critical patent/JPH03284607A/en
Application granted granted Critical
Publication of JP2849437B2 publication Critical patent/JP2849437B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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
    • A61K8/04—Dispersions; Emulsions
    • A61K8/06—Emulsions
    • 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
    • A61K8/11—Encapsulated compositions
    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/63—Steroids; Derivatives thereof
    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/64—Proteins; Peptides; Derivatives or degradation products thereof
    • A61K8/65—Collagen; Gelatin; Keratin; Derivatives or degradation products thereof
    • 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
    • A61K8/73—Polysaccharides
    • A61K8/735—Mucopolysaccharides, e.g. hyaluronic acid; Derivatives thereof
    • 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
    • B01F23/40—Mixing liquids with liquids; Emulsifying
    • B01F23/41—Emulsifying
    • B01F23/4105—Methods of emulsifying
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02—Making microcapsules or microballoons
    • B01J13/025—Applications of microcapsules not provided for in other subclasses
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02—Making microcapsules or microballoons
    • B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
    • B01J13/046—Making microcapsules or microballoons by physical processes, e.g. drying, spraying combined with gelification or coagulation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
    • B05B11/0005—Components or details
    • B05B11/0078—Arrangements for separately storing several components
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
    • B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
    • B05B11/02—Membranes or pistons acting on the contents inside the container, e.g. follower pistons
    • B05B11/028—Pistons separating the content remaining in the container from the atmospheric air to compensate underpressure inside the container
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
    • B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
    • B05B11/10—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle
    • B05B11/1001—Piston pumps
    • B05B11/1023—Piston pumps having an outlet valve opened by deformation or displacement of the piston relative to its actuating stem
    • B05B11/1026—Piston pumps having an outlet valve opened by deformation or displacement of the piston relative to its actuating stem the piston being deformable and its deformation allowing opening of the outlet
    • 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
    • A61K2800/41—Particular ingredients further characterized by their size
    • A61K2800/412—Microsized, i.e. having sizes between 0.1 and 100 microns
    • 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
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88—Two- or multipart kits

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Colloid Chemistry (AREA)
  • Medicinal Preparation (AREA)

Description

【発明の詳細な説明】 〔発明の目的〕 ａ）産業上の利用分野 本発明は、化粧クリームや化粧乳液類等の乳化状の化
粧品と医薬部外品に関するものである。The present invention relates to emulsified cosmetics such as cosmetic creams and cosmetic emulsions and quasi-drugs.

ｂ）従来の技術 従来のこの種の乳化化粧品等は、組成上で大別すると
脂肪酸，油脂，蝋等による油脂成分と、保湿剤，精製水
等による水溶液成分と、両成分間に介在されて乳化や分
散を助勢する界面活性剤と、油脂成分のための酸化防止
剤等で構成され、前記油脂成分と水溶液成分並びに界面
活性剤をバランス良く配合して加温乳化したものを容器
内へ混合状態で一体に収納したものである。b) Conventional technology Conventionally, this type of emulsified cosmetics and the like can be roughly classified in terms of composition, such as fatty components such as fatty acids, fats and waxes, and aqueous components such as humectants and purified water. A surfactant that assists emulsification and dispersion, and an antioxidant for fats and oils, etc., is mixed into a container after warming and emulsifying the fats and oils, the aqueous solution, and the surfactant in a well-balanced manner. It is housed integrally in the state.

この内の界面活性剤は、商品の品質を安定化させるた
めに不可欠のものであり、特に乳液タイプの商品ほど界
面活性剤の配合バランスが商品の品質を決定する大きな
要素となっている。また酸化防止剤は、商品の主要成分
である油脂成分が空気や紫外線等によって酸化して品質
が劣化しやすいので、これを防止するために配合されて
いる。Among them, the surfactant is indispensable for stabilizing the quality of the product. In particular, the balance of the surfactant is a major factor in determining the quality of the product as the product is of the emulsion type. The antioxidant is incorporated in order to prevent the oil and fat component, which is a main component of the product, from being oxidized by air, ultraviolet rays, and the like to easily deteriorate the quality.

ｃ）発明が解決しようとする課題 ところで、前記した界面活性剤や酸化防止剤等は皮膚
にとってはあまり好ましいものではなく、なるべくなら
ば使用を差し控えたい成分であるが、従来の乳化化粧品
等ではこれらを配合させないと、保存中に油脂成分と水
溶液成分とが分離したり酸化によって油脂成分が変質し
たりして商品の品質を著しく劣化させる。c) Problems to be Solved by the Invention Incidentally, the above-mentioned surfactants and antioxidants are not so preferable for the skin, and are components which should not be used as much as possible. If not mixed, the oil and fat component and the aqueous solution component are separated during storage, and the oil and fat component is deteriorated by oxidation, so that the quality of the product is significantly deteriorated.

そこで本発明では、界面活性剤や酸化防止剤等の使用
を最小限度に押えて皮膚に対するトラブルを防止すると
共に、保存中に商品の品質が劣化されることなく安定さ
せることができるようにした化粧クリームや化粧乳液類
等のように洗い落ししない乳化状の化粧品と医薬部外品
の提供を目的とするものである。Therefore, in the present invention, a cosmetic that can minimize the use of surfactants and antioxidants to prevent troubles on the skin and stabilize the product without deterioration during storage. An object of the present invention is to provide emulsified cosmetics and quasi-drugs that do not wash off, such as creams and cosmetic emulsions.

〔発明の構成〕[Configuration of the invention]

ａ）課題を解決するための手段 本発明の要旨は、カンテンとカプセル破壊剤を精製水
に混合して造られたカプセル内に油脂成分が封入された
カプセルベースと、このカプセルベースを水溶液成分中
に浮遊状態で混在させて収納する容器とで構成され、前
記容器には取り出す際に前記カプセルを細断して油脂成
分と水溶液成分を強制混合して乳化させると共に、細断
したカプセルを前記カプセル破壊剤で微粒状に分散させ
て取り出す取出し機構を装着したことを特徴とする乳化
状の化粧品と医薬部外品であり、前記カプセル破壊剤と
しては粉末顔料の使用が望ましい。a) Means for Solving the Problems The gist of the present invention is to provide a capsule base in which a fat and oil component is encapsulated in a capsule made by mixing agar and a capsule breaking agent into purified water; A container that is mixed and stored in a floating state, and when the container is taken out, the capsule is shredded, the fat and oil component and the aqueous solution component are forcibly mixed and emulsified, and the shredded capsule is cut into the capsule. Emulsified cosmetics and quasi-drugs are provided with a take-out mechanism that disperses and disperses them into fine particles with a disintegrating agent, and powder pigment is desirable as the capsule-disintegrating agent.

また、前記取出し機構としては、所定量のカプセルベ
ースと水溶液成分を貯留する貯留室に対し、常時は上限
位置にバネ付勢されて操作キャップの押圧操作で下限位
置へ移行される摺動杆の下端部を出没可能に突出させる
と共に、当該貯留室を前記容器に連通させる流入路及び
噴射ノズルに連通させる流出路をそれぞれ設け、前記流
出路側には下限位置へ移行する摺動杆の下端部が前記貯
留室内のカプセルベースと水溶液成分を圧縮した際に開
き、当該貯留室内からカプセルベースと水溶液成分の流
出を可能にする弁部材を設け、前記流入路側にはバネ復
帰して上限位置へ移行する摺動杆の下端部が前記貯留室
内を負圧にした際に開き、前記容器から新たなカプセル
ベースと水溶液成分を吸引して流入を可能にする弁部材
を設け、前記貯留室内には流出するカプセルベースが通
過する際にカプセルを細断する手段を設けた構造が望ま
しい。In addition, the take-out mechanism includes a sliding rod which is normally biased to an upper limit position and moved to a lower limit position by a pressing operation of an operation cap with respect to a storage chamber for storing a predetermined amount of capsule base and an aqueous solution component. The lower end is projected so as to be able to protrude and retract, and an inflow path for communicating the storage chamber with the container and an outflow path for communicating with the injection nozzle are respectively provided.On the outflow path side, a lower end of a sliding rod moving to a lower limit position is provided. A valve member that opens when the capsule base and the aqueous solution component in the storage chamber is compressed and allows the capsule base and the aqueous solution component to flow out of the storage chamber is provided, and a spring returns to the inflow path side to move to the upper limit position. A lower end portion of the sliding rod is opened when the pressure in the storage chamber is reduced to a negative pressure, and a new capsule base and a valve member are provided for allowing a new aqueous solution component to flow in from the container; Structure provided with means for shredding the capsule when the capsule base flowing passes in desirable.

更に、前記取出し機構における前記カプセルを細断す
る手段としては、前記摺動杆を上限位置にバネ付勢する
ために、当該摺動杆の下端部に上端側を巻装して前記貯
留室内に収容させたコイルスプリングを兼用することが
できる。Further, as means for shredding the capsule in the take-out mechanism, in order to bias the sliding rod to the upper limit position, an upper end side is wound around a lower end of the sliding rod, and the capsule is inserted into the storage chamber. The accommodated coil spring can also be used.

ｂ）実施例 以下に、本発明を実施例に基づいて説明する。この乳
化化粧品等は、第１図のようにカンテンを主成分とした
カプセル１内に油脂成分２が封入されたカプセルベース
３と水溶液成分４とが容器本体５内に一緒に収納され、
このカプセルベース３は常時は水溶液成分４中に浮遊状
態で点在している。前記容器本体５には、使用時にカプ
セルを細断した状態にして容器４内からカプセルベース
３と水溶液成分４とを取り出すことができる取出し機構
６が設けられ、これにより両成分2,4が瞬時に強制混合
され乳化状態で取り出されるようにしている。b) Examples Hereinafter, the present invention will be described based on examples. In this emulsified cosmetic or the like, a capsule base 3 in which an oil or fat component 2 is enclosed in a capsule 1 containing agar as a main component and an aqueous solution component 4 are housed together in a container body 5 as shown in FIG.
The capsule base 3 is usually scattered in the aqueous solution component 4 in a floating state. The container main body 5 is provided with a take-out mechanism 6 that can take out the capsule base 3 and the aqueous solution component 4 from the inside of the container 4 by shredding the capsule at the time of use. Forcibly mixed and taken out in an emulsified state.

前記カプセル１は、加温した精製水にカンテンと増粘
剤を混合して溶解させ、これに粉末顔料を加えて良く混
合したものである。この内のカンテンは、カプセル１を
成形するための主原料であり、前記水溶液成分４から油
脂成分２を保護して安定的に保存させるためのものであ
る。また増粘剤は、カプセル１を成形するカンテン被膜
の強度を調整するための助剤であって、例えばアルギン
酸ナトリウム等が使用される。更に粉末顔料はカプセル
破壊剤として使用され、カプセル１が細断された際にカ
ンテン被膜を破壊分散させてカンテンの粕が無くなる状
態にまで微粒状にするものであり、例えばセリサイト，
雲母チタン，酸化チタン等の粉末顔料が使用されるが、
タルクや酸化カルシウム等の化粧用粉末顔料の使用も可
能である。The capsule 1 is obtained by mixing and dissolving agar and a thickener in heated purified water, adding a powdered pigment thereto, and mixing well. The agar in this is a main raw material for forming the capsule 1, and is for protecting the oil component 2 from the aqueous solution component 4 and stably storing it. The thickener is an auxiliary agent for adjusting the strength of the agar film forming the capsule 1, and for example, sodium alginate or the like is used. Further, the powdered pigment is used as a capsule breaking agent, and when the capsule 1 is shredded, the agar coating is broken and dispersed to form fine particles until the agar powder is eliminated.
Powder pigments such as titanium mica and titanium oxide are used,
It is also possible to use cosmetic powder pigments such as talc and calcium oxide.

次に前記カプセル１に封入される油脂成分２は、例え
ばスクワランやホホバ油等の油脂やステアリン酸やミリ
チン酸等の脂肪酸と、例えばトリオクタン酸グリセリル
等の中性脂肪酸と、ヒドロキステアリン酸コレステリン
やレシチン等の必要に応じて添加される乳化助剤と、天
然ビタミンＥや香料等の添加剤を成分とする。この内で
中性脂肪酸であるトリオクタン酸グリセリルは比重調整
剤として使用され、前記したようにカプセルベース３を
水溶液成分４中で浮遊状態にさせるために比重を9.0〜
9.8に調整している。Next, the fat component 2 encapsulated in the capsule 1 includes, for example, fats and oils such as squalane and jojoba oil, fatty acids such as stearic acid and myritic acid, neutral fatty acids such as glyceryl trioctanoate, and cholesterol hydroxtearate. The ingredients include an emulsifying aid, such as lecithin, which is added as needed, and additives, such as natural vitamin E and flavors. Among these, glyceryl trioctanoate, which is a neutral fatty acid, is used as a specific gravity adjusting agent, and has a specific gravity of 9.0 to 9 to suspend the capsule base 3 in the aqueous solution component 4 as described above.
Adjusted to 9.8.

前記油脂成分２をカプセル１に封入させるのには、例
えば冷却液中に二重ノズルを埋設し、内筒内に前記油脂
成分２を内筒と外筒間に前記カプセル成分を各々加温し
て溶融状態で注入し、その際に超音波振動を与えると前
記カプセル成分が球状に変形されてカプセル１が形成さ
れ、その内部に油脂成分２が真空状態で封入される。こ
のカプセルベース３は、例えば３Φ程度の球状でカプセ
ルの被膜率は30〜90％であって、望ましくはカプセル１
の重量パーセント70に対して油性成分２は30％とする。In order to enclose the fat / oil component 2 in the capsule 1, for example, a double nozzle is buried in a cooling liquid, and the fat / oil component 2 is heated in the inner cylinder between the inner cylinder and the outer cylinder. When the mixture is injected in a molten state and ultrasonic vibration is applied at that time, the capsule component is deformed into a spherical shape to form a capsule 1 and the oil component 2 is sealed therein in a vacuum state. The capsule base 3 has a spherical shape of, for example, about 3Φ, and has a capsule coverage of 30 to 90%.
The oily component 2 is 30% based on 70% by weight of

次に前記水溶液成分４は、精製水にカルボキシンビニ
ルポリマー等の増粘剤を混合状態で溶解させ、これに水
酸化ナトリウム等の増粘調整剤を混合して中和させた水
溶液に、保湿剤等の添加剤を順次混合して造られる。Next, the aqueous solution component 4 is prepared by dissolving a thickener such as a carboxin vinyl polymer in purified water in a mixed state, and mixing with a thickener such as sodium hydroxide to neutralize the aqueous solution. It is produced by sequentially mixing additives such as agents.

これらの添加剤としては、例えば濃グリセリンやジプ
ロピレングリコール等の保湿剤と、アテロコラーゲンや
バイオヒアルロン酸等の天然高分子保湿剤と、クエン酸
ナトリウム等のPH緩衝剤と、アルコール等の防腐助剤
と、パラオキシル安息香酸エステルやフェノキシエタノ
ール等の防腐剤が使用される。Examples of these additives include humectants such as concentrated glycerin and dipropylene glycol, natural polymer humectants such as atelocollagen and biohyaluronic acid, PH buffering agents such as sodium citrate, and preservative aids such as alcohol. And preservatives such as paraoxyl benzoate and phenoxyethanol.

そして、前記容器本体５内にカプセルベース３と水溶
液成分５とが例えば各50％の割合で収容される。この場
合に、カプセルベース３は前記比重調整剤によって比重
が9.0〜9.8に調整されているので、水溶液成分４中の上
部側に浮遊状態で混在して保存されている。Then, the capsule base 3 and the aqueous solution component 5 are accommodated in the container body 5 at a ratio of, for example, 50%. In this case, since the specific gravity of the capsule base 3 is adjusted to 9.0 to 9.8 by the specific gravity adjusting agent, the capsule base 3 is stored in a suspended state on the upper side in the aqueous solution component 4.

次に収納容器の全体構造に付いて第１図乃至第４図で
説明する。Next, the overall structure of the storage container will be described with reference to FIGS.

容器本体５は、ガラスまたは硬質合成樹脂材によって
上下が開口する円筒状に形成され、望ましくは残存量が
確認できるように透明または半透明にしておくと良い。
この容器本体５の下部側開口は、当該開口内に嵌挿され
た可撓性を有する合成ゴム材等で形成された密封栓７と
開閉蓋８によって閉塞されている。密封栓７は、二重筒
状で外筒の上下端部から環状の摺動片7a,7bが各々突設
され、内筒には開閉蓋８が被着される。尚、符号９は容
器本体５の下端部に被着される保護キャップである。The container main body 5 is formed of glass or a hard synthetic resin material into a cylindrical shape having an open top and bottom, and is desirably transparent or translucent so that the remaining amount can be confirmed.
The lower opening of the container main body 5 is closed by a sealing stopper 7 and a lid 8 made of a flexible synthetic rubber material or the like fitted in the opening. The sealing plug 7 has a double cylindrical shape, and annular sliding pieces 7a and 7b are respectively protruded from upper and lower ends of an outer cylinder, and an opening / closing lid 8 is attached to the inner cylinder. Reference numeral 9 denotes a protective cap attached to the lower end of the container body 5.

容器本体５の上部側開口には前記したようにカプセル
を細断状態で取出しする取出し機構６が装着されてい
る。この取出し機構６は、案内筒10,吸引筒11等の静止
部材と、摺動杆12,弁筒13,押圧筒14,操作キャップ15等
の可動部材と、ボール16,コイルスプリング17,シールパ
ッキン18,保持リング19等の中間部材とで構成されてい
る。As described above, the take-out mechanism 6 that takes out the capsule in a chopped state is attached to the upper opening of the container body 5. The take-out mechanism 6 includes stationary members such as a guide cylinder 10 and a suction cylinder 11, movable members such as a sliding rod 12, a valve cylinder 13, a pressing cylinder 14, and an operation cap 15, a ball 16, a coil spring 17, and a seal packing. 18, and an intermediate member such as a holding ring 19.

前記シールパッキン18は環状で容器本体５の上部側開
口縁部に載置され、このシールパッキン18には二重筒状
の案内筒10の外筒側が載置され、当該案内筒10の外筒側
と容器本体５の上端部側を挾持する態様で保持リング19
が可締め付けている。前記吸引筒11は順次縮径する多段
状の筒状体で、上端部側が案内筒10の内外筒間に挿入さ
れて当該上端部が案内筒10に係止され、中間部にはステ
ンレスや硬質合成樹脂等によるボール16が遊動自在に収
容されている。The seal packing 18 is annularly mounted on the upper opening edge of the container body 5, and the outer cylinder side of the double cylindrical guide cylinder 10 is mounted on the seal packing 18. The holding ring 19 is held in such a manner that the
Are tightenable. The suction cylinder 11 is a multi-stage cylindrical body whose diameter is sequentially reduced, and the upper end is inserted between the inner and outer cylinders of the guide cylinder 10 and the upper end is locked by the guide cylinder 10. A ball 16 made of a synthetic resin or the like is freely movably accommodated.

前記押圧筒14は上部側が小径で下部側が大径な筒状体
で、当該下部側が前記案内筒10の内筒へ昇降可能に挿入
されると共に、下端部は案内筒10に係合されている。前
記摺動杆12は中間部の外周に環状フランジ12aが突設さ
れた円柱状で、周面に複数の縦溝12bが刻設されている
上部側が前記押圧筒14の大径筒内に挿入されている。ま
た、摺動杆12の下部側の外周には上端部が環状フランジ
12aに係合された前記コイルスプリング17が巻装され、
当該コイルスプリング17の下端部は前記吸引筒12内の段
部に係合されて摺動杆12を上方へ付勢している。更に、
前記弁筒12は柔軟な合成樹脂材で形成され、上端部が前
記押圧筒14の下端部に固着されると共に、下端部側の外
周が前記吸引筒11の内面を摺接する態様で摺動杆12の中
間部の外周囲に設けられている。The pressing cylinder 14 is a cylindrical body having a small diameter on the upper side and a large diameter on the lower side, and the lower side is inserted into the inner cylinder of the guide cylinder 10 so as to be able to move up and down, and the lower end is engaged with the guide cylinder 10. . The sliding rod 12 has a columnar shape with an annular flange 12a protruding from an outer periphery of an intermediate portion, and a plurality of vertical grooves 12b are engraved on a peripheral surface, and an upper side thereof is inserted into a large-diameter cylinder of the pressing cylinder 14. Have been. The upper end of the outer periphery of the lower side of the sliding rod 12 is an annular flange.
The coil spring 17 engaged with 12a is wound,
The lower end of the coil spring 17 is engaged with a step in the suction tube 12 to urge the sliding rod 12 upward. Furthermore,
The valve cylinder 12 is formed of a flexible synthetic resin material, and has an upper end portion fixed to a lower end portion of the pressing cylinder 14 and a sliding rod whose outer periphery on the lower end side is in sliding contact with the inner surface of the suction cylinder 11. It is provided around the outer periphery of the middle part of the twelve.

前記操作キャップ15は、二重筒状で内筒に連通してノ
ズル15aが形成され、内外筒間が前記案内筒10の内外筒
間へ摺動可能に嵌合されると共に、内筒内には前記押圧
筒14の小径な上部筒が圧入状態で固着されている。The operation cap 15 is formed in a double cylindrical shape and communicates with the inner cylinder to form a nozzle 15a, and the inner and outer cylinders are slidably fitted between the inner and outer cylinders of the guide cylinder 10, and are inserted into the inner cylinder. Is fixed to a small-diameter upper cylinder of the pressing cylinder 14 in a press-fit state.

前記の取出し機構６が装着された容器本体５内には、
密封栓７から開閉蓋８を取り外して前記カプセルベース
３と水溶液成分４とが混在状態で充填される。この充填
されたカプセルベース３はカンテンを主材としたカプセ
ル１によって油脂成分２の酸化が防止されているので、
従来の乳化化粧品等のように酸化防止剤の添加が不要が
極めて小量で良いと共に、油脂成分２と水溶液成分４を
乳化状態で混合させておく必要がないので界面活性剤の
添加も不要か極めて小量で良い。In the container body 5 to which the above-mentioned take-out mechanism 6 is attached,
The lid 8 is removed from the sealing stopper 7, and the capsule base 3 and the aqueous solution component 4 are filled in a mixed state. Since the filled capsule base 3 prevents oxidation of the fat component 2 by the capsule 1 mainly composed of agar,
Unlike the conventional emulsified cosmetics, it is not necessary to add an antioxidant and a very small amount is required. In addition, since it is not necessary to mix the oil component 2 and the aqueous solution component 4 in an emulsified state, it is unnecessary to add a surfactant. An extremely small amount is sufficient.

この容器本体５に装着された取出し機構６は、常時は
第１図のようにコイルスプリング17によって上方へ付勢
された摺動杆12に押圧筒14と操作キャップ５が押し上げ
られた上限位置になっている。また、使用時に指先で操
作キャップ15を押圧するとコイルスプリング17の弾撥力
に抗して摺動杆12が下動して第２図の下限位置まで降下
され、この状態で指先による押圧力を取り除くと第１図
の上限位置へ復帰する。The unloading mechanism 6 mounted on the container body 5 is always in the upper limit position where the pressing cylinder 14 and the operation cap 5 are pushed up by the sliding rod 12 urged upward by the coil spring 17 as shown in FIG. Has become. When the operation cap 15 is pressed with the fingertip during use, the sliding rod 12 moves downward against the resilience of the coil spring 17 and is lowered to the lower limit position in FIG. 2, and in this state, the pressing force by the fingertip is reduced. When removed, it returns to the upper limit position in FIG.

前記した上限位置の状態では、前記摺動杆12の環状フ
ランジ12aに内面が密接された弁筒13と、この弁筒13の
外面が密接状態で摺接される吸引筒11とで形成される貯
溜室20内に、後述するようにして吸引された所定量のカ
プセルベース３と水溶液成分４とが既に収納されてい
る。この取出し機構６を下限位置の状態へ移行させる
と、途中で貯溜室20内のカプセルベース３と水溶液成分
４とは順次圧縮され、下限位置の状態では前記吸引筒11
の段部に弁筒13の下端部に係止されて第３図のように拡
開し、密接していた弁筒13の内面と摺動杆12の環状フラ
ンジ12aとの間にギャップが生じて遮断されていた当該
摺動杆12の上部側と下部側とが連通する。従って、それ
まで圧縮されていた貯溜室20内のカプセルベース３と水
溶液成分４とが摺動杆12の縦溝12bと押圧筒14の内部を
通って操作キャップ15のノズル15aから噴射される。In the state of the upper limit position described above, a valve cylinder 13 whose inner surface is in close contact with the annular flange 12a of the sliding rod 12 and a suction tube 11 in which the outer surface of the valve cylinder 13 is in close contact with the sliding member are formed. A predetermined amount of the capsule base 3 and the aqueous solution component 4 sucked in a manner described later are already stored in the storage chamber 20. When the take-out mechanism 6 is shifted to the lower limit position, the capsule base 3 and the aqueous solution component 4 in the storage chamber 20 are sequentially compressed on the way.
At the stepped portion, the lower end of the valve cylinder 13 is locked and expanded as shown in FIG. 3, and a gap is formed between the inner surface of the valve cylinder 13 and the annular flange 12a of the sliding rod 12 which were in close contact. The upper side and the lower side of the sliding rod 12 that has been blocked by the communication are communicated with each other. Accordingly, the capsule base 3 and the aqueous solution component 4 in the storage chamber 20 which have been compressed up to that time are jetted from the nozzle 15a of the operation cap 15 through the vertical groove 12b of the sliding rod 12 and the inside of the pressing cylinder 14.

次に、コイルスプリング17の弾撥力によって前記した
取出し機構６が上限位置の状態へ移行を開始すると、弁
筒13は縮径して第４図のように再び摺動杆12の環状フラ
ンジ12aに密接され、貯溜室20内の負圧状態を解消する
ように容器本体５内のカプセルベース３と水溶液成分４
とがボール16を押上ながら吸引筒11を介して貯溜室20内
へ吸引される。このカプセルベース３と水溶液成分４と
がコイルスプリング17を通過する際に、カプセル１が当
該コイルスプリング17によって細断され、封入されてい
た油脂成分２が水溶液成分４と強制混合されて乳化する
と共に、カプセル成分に含有されていた粉末顔料等によ
るカプセル破壊剤が、カンテンの結合分子を破壊して微
粒状に分散させる。従って、取出し機構６が上限位置の
状態へ移行を完了するまでの貯溜室20内には、上部側に
乳化状態で下部側はカプセルベース３と水溶液成分４と
に分離した状態に所定量が貯溜される。これらは次に下
限位置の状態へ移行される際に前記のようにノズル15a
から噴射されるが、その際に下部側のカプセルベース３
はコイルスプリング17を通過して細断された状態でノズ
ル15aから噴射される。Next, when the take-out mechanism 6 starts to move to the upper limit position by the elastic force of the coil spring 17, the valve cylinder 13 is reduced in diameter and the annular flange 12a of the sliding rod 12 is again reduced as shown in FIG. And the capsule base 3 in the container body 5 and the aqueous solution component 4 so as to eliminate the negative pressure state in the storage chamber 20.
Are sucked into the storage chamber 20 via the suction tube 11 while pushing up the ball 16. When the capsule base 3 and the aqueous solution component 4 pass through the coil spring 17, the capsule 1 is shredded by the coil spring 17, and the encapsulated oil and fat component 2 is forcibly mixed with the aqueous solution component 4 and emulsified. In addition, a capsule breaking agent such as a powder pigment contained in the capsule component breaks the binding molecules of the agar and disperses them into fine particles. Therefore, a predetermined amount is stored in the storage chamber 20 until the take-out mechanism 6 completes the transition to the state of the upper limit position, in a state where the upper side is emulsified and the lower side is separated into the capsule base 3 and the aqueous solution component 4. Is done. These are used when the nozzle 15a is moved to the lower limit position as described above.
From the capsule base 3 on the lower side
Is ejected from the nozzle 15a in a state of being cut through the coil spring 17.

尚、前記密封栓７は環状の摺動片7a,7bが容器本体５
の内面に密接して収納されているカプセルベース３と水
溶液成分４が漏洩しないようにするだけではなく、容器
本体５内からカプセルベース３と水溶液成分５とが順次
取り出されて収納量が減少する毎に、第２図のように上
部開口側へ順次摺動し、カプセルベース３と水溶液成分
４の取り出しが容易になるように成っている。The sealing plug 7 has annular sliding pieces 7a and 7b which are
In addition to not only preventing the capsule base 3 and the aqueous solution component 4 housed in close contact with the inner surface of the container from leaking, the capsule base 3 and the aqueous solution component 5 are also sequentially taken out from the container body 5 to reduce the storage amount. Each time, the capsule base 3 and the aqueous solution component 4 are easily slid to the upper opening side as shown in FIG.

更に、本発明は前記した実施例に限定されるものでは
なく、要旨の範囲内で各種の変形を採り得るものであ
る。例えば第５図のように収納する容器本体21を柔軟性
のある合成樹脂のチューブとし、この容器本体21の取出
し口の途中を膨出させて貯溜室22を形成させると共に、
当該貯溜室22の入り口にボール23を挿入し、取出し口に
はチューブから押出されたカプセルベース３を細断する
メッシュ状の細断筒を設ける構成もある。尚、符号24は
キャップである。Further, the present invention is not limited to the above-described embodiment, and can adopt various modifications within the scope of the gist. For example, as shown in FIG. 5, the container main body 21 to be housed is a flexible synthetic resin tube, and the storage chamber 22 is formed by expanding the middle of the outlet of the container main body 21,
There is also a configuration in which a ball 23 is inserted into the inlet of the storage chamber 22, and a mesh-shaped shredder that shreds the capsule base 3 extruded from the tube is provided at the outlet. Reference numeral 24 denotes a cap.

最後に、この乳化化粧品等の成分配合例を示す。（カ
プセル成分） 精製水 88.00 カンテン（カプセル主原料） 1.50 アルギン酸ナトリウム（カプセル成形助剤） 1.50 セリサイト（粉末顔料） 4.00 雲母チタン（粉末顔料） 2.50 酸化チタン（粉末顔料） 2.50 （カプセル内容物成分） トリオクタン酸グリセリル（比重調整剤） 49.67 ホホバ油（オイル主原料） 30.00 スクワラン（オイル主原料） 20.00 ヒドロキシステアリン酸コレステリル（乳化助剤）
0.10 グリチルレチン酸ステアリル（消炎剤） 0.05 天然ビタミンＥ（天然酸化防止剤） 0.05 パラオキシ安息香酸エステル（防腐剤） 0.03 香料 0.10 （乳化化粧品） カプセルベース（カプセル成分＋カプセル内容物成
分） 50.00 精製水 43.055 カルボキシビニルポリマー（増粘剤） 0.100 水酸化ナトリウム（増粘調整剤） 0.025 濃グリセリン（保湿剤） 2.500 ジプロピレングリコール（保湿剤） 2.500 アテロコラーゲン（天然高分子保湿剤） 0.100 バイオヒアルロン酸（天然高分子保湿剤） 0.100 クエン酸ナトリウム（PH緩衝剤） 0.010 アルコール（防腐助剤） 1.500 パラオキシ安息香酸エステル（防腐剤） 0.060 フェノキシエタノール（防腐剤） 0.050 〔発明の効果〕 前記した実施例でも明らかなとおり、本発明の乳化状
の化粧品と医薬部外品では、カンテンを主材としたカプ
セル内に油脂成分を封入してカプセルベースを造り、こ
のカプセルベースが水溶液成分と一緒に容器内に収納し
て保存されるので、カプセルによって油脂成分の酸化が
防止されて従来の乳化化粧品等に比べて添加させる酸化
防止剤の量を著しく少なくすることができる。Finally, an example of the composition of the components for the emulsified cosmetics and the like will be described. (Capsule component) Purified water 88.00 Agar (capsule main raw material) 1.50 Sodium alginate (capsule forming aid) 1.50 Sericite (powder pigment) 4.00 Titanium mica (powder pigment) 2.50 Titanium oxide (powder pigment) 2.50 (capsule content component) Glyceryl trioctanoate (specific gravity adjuster) 49.67 Jojoba oil (oil main ingredient) 30.00 Squalane (oil main ingredient) 20.00 Cholesteryl hydroxystearate (emulsifier)
0.10 Stearyl glycyrrhetinate (anti-inflammatory) 0.05 Natural vitamin E (natural antioxidant) 0.05 Paraoxybenzoate (preservative) 0.03 Fragrance 0.10 (Emulsified cosmetics) Capsule base (capsule component + capsule content component) 50.00 Purified water 43.055 carboxy Vinyl polymer (thickener) 0.100 Sodium hydroxide (thickener) 0.025 Concentrated glycerin (humectant) 2.500 Dipropylene glycol (humectant) 2.500 Atelocollagen (natural polymer humectant) 0.100 Biohyaluronic acid (natural polymer moisturizer) Agent) 0.100 Sodium citrate (PH buffer) 0.010 Alcohol (preservative aid) 1.500 Paraoxybenzoate (preservative) 0.060 Phenoxyethanol (preservative) 0.050 [Effects of the invention] As is clear from the above-described examples, the present invention is In emulsified cosmetics and quasi-drugs, the main ingredient is agar The capsule base is made by enclosing the fat and oil components in the capsule and the capsule base is stored and stored in the container together with the aqueous solution component. The amount of antioxidant to be added can be remarkably reduced as compared with the above.

また、前記カプセルベースは使用時に収納容器から取
り出すと、装着した取出し機構中でカプセルを細断して
内部の油脂成分を水溶液成分に強制混合して乳化させた
状態で取り出されるので、油脂成分と水溶液成分とを予
め乳化状態で混合させておく従来の乳化化粧品等とは異
なり界面活性剤の添加が不要または量を著しく少なくす
ることができる。Further, when the capsule base is taken out of the storage container at the time of use, the capsule is shredded in the attached take-out mechanism, and the grease component inside is forcibly mixed with the aqueous solution component and taken out in an emulsified state. Unlike a conventional emulsified cosmetic product or the like in which an aqueous solution component is previously mixed in an emulsified state, the addition of a surfactant is unnecessary or the amount can be significantly reduced.

従って、肌を損なうことのない良質の乳化化粧品等が
得られると共に、細断されたカプセル成分は混合されて
いる粉末顔料等によるカプセル破壊剤によって微粒状に
分散されるので塗布が滑らかで、一旦塗った後で洗い落
とすことのないクリームや乳液等の乳化状の化粧品と医
薬部外品には極めて有効である。Accordingly, a high-quality emulsified cosmetic product without damaging the skin can be obtained, and the shredded capsule components are dispersed in fine particles by a capsule breaking agent such as a powdered pigment that is mixed, so that the application is smooth, and the coating is smooth. It is extremely effective for emulsified cosmetics and quasi-drugs such as creams and emulsions that do not wash off after being applied.

また、取出し機構として請求項（２）のような構成を
採ると、適量づつを乳化させた状態で容易に取り出すこ
とができ、特に請求項（３）のように取出し機構の復帰
用バネであるコイルスプリングを細断する手段としても
兼用させると、格別な細断機構を設ける必要が無く装置
を簡単にすることができる。In addition, when the take-out mechanism is configured as in claim (2), an appropriate amount can be easily taken out in an emulsified state. In particular, the take-out mechanism is a return spring of the take-out mechanism. If the coil spring is also used as a means for shredding, the device can be simplified without having to provide a special shredding mechanism.

【図面の簡単な説明】[Brief description of the drawings]

第１図と第２図は、本発明の実施例による容器に収納さ
れた乳化化粧品等の全体縦断面図で、第１図は取出し機
構が上限位置の状態を第２図は取出し機構が下限位置の
状態を各々示し、第３図はは乳化化粧品等の取出し状態
を説明する要部拡大縦断面図、第４図は乳化化粧品等の
吸引状態を説明する要部拡大縦断面図、第５図は本発明
の他の実施例による容器に収納された乳化化粧品等の全
体縦断面図である。 〔符号の説明〕 １……カプセル、２……油脂成分 ３……カプセルベース、４……水溶液成分 ５……容器本体、６……取出し機構 ７……密封栓、８……開閉蓋 ９……保護キャップ、10……案内筒 11……吸引筒、12……摺動杆 13……弁筒、14……押圧筒 15……操作キャップ、16……ボール 17……コイルスプリング、18……シールパッキン 19……保持リング、20……貯溜室 21……容器本体、22……貯溜室 23……ボール、24……キャップ1 and 2 are overall longitudinal sectional views of an emulsified cosmetic or the like stored in a container according to an embodiment of the present invention. FIG. 1 shows a state in which the take-out mechanism is at an upper limit position, and FIG. FIG. 3 is an enlarged vertical cross-sectional view of a main part illustrating a state of taking out emulsified cosmetics and the like, FIG. 4 is an enlarged vertical cross-sectional view of a main part illustrating a suction state of emulsified cosmetics and the like, FIG. The figure is an overall longitudinal sectional view of an emulsified cosmetic product or the like stored in a container according to another embodiment of the present invention. [Description of References] 1 capsule 2 oil component 3 capsule base 4 aqueous solution component 5 container body 6 take-out mechanism 7 sealing stopper 8 opening / closing lid 9 ... Protective cap, 10 ... Guide cylinder 11 ... Suction cylinder, 12 ... Sliding rod 13 ... Valve cylinder, 14 ... Pressing cylinder 15 ... Operation cap, 16 ... Ball 17 ... Coil spring, 18 ... … Seal packing 19… Retaining ring, 20… Storage chamber 21… Container body, 22… Storage chamber 23… Ball, 24… Cap

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項１】カンテンとカプセル破壊剤を精製水に混合
して造られたカプセル内に油脂成分が封入されたカプセ
ルベースと、このカプセルベースを水溶液成分中に浮遊
状態で混在させて収納する容器とで構成され、前記容器
には取り出す際に前記カプセルを細断して油脂成分と水
溶液成分を強制混合して乳化させると共に、細断したカ
プセルを前記カプセル破壊剤で微粒状に分散させて取り
出す取出し機構を装着したことを特徴とする乳化状の化
粧品と医薬部外品。1. A capsule base in which a fat component is enclosed in a capsule made by mixing agar and a capsule breaking agent with purified water, and a container for containing the capsule base in a suspended state in an aqueous solution component When taken out into the container, the capsule is shredded, the fat and oil component and the aqueous solution component are forcibly mixed and emulsified, and the shredded capsule is dispersed in the form of fine particles with the capsule breaking agent and taken out. Emulsified cosmetics and quasi-drugs equipped with a take-out mechanism. 【請求項２】前記取出し機構は、所定量のカプセルベー
スと水溶液成分を貯留する貯留室に対し、常時は上限位
置にバネ付勢されて操作キャップの押圧操作で下限位置
へ移行される摺動杆の下端部を出没可能に突出させると
共に、当該貯留室を前記容器に連通させる流入路及び噴
射ノズルに連通させる流出路をそれぞれ設け、前記流出
路側には下限位置へ移行する摺動杆の下端部が前記貯留
室内のカプセルベースと水溶液成分を圧縮した際に開
き、当該貯留室内からカプセルベースと水溶液成分の流
出を可能にする弁部材を設け、前記流入路側にはバネ復
帰して上限位置へ移行する摺動杆の下端部が前記貯留室
内を負圧にした際に開き、前記容器から新たなカプセル
ベースと水溶液成分を吸引して流入を可能にする弁部材
を設け、前記貯留室内には流出するカプセルベースが通
過する際にカプセルを細断する手段を設けた請求項
（１）に記載の乳化状の化粧品と医薬部外品。2. The sliding mechanism according to claim 1, wherein said take-out mechanism is always urged to an upper limit position by a spring to a storage chamber for storing a predetermined amount of a capsule base and an aqueous solution component, and is shifted to a lower limit position by a pressing operation of an operation cap. A lower end of the sliding rod is provided so as to protrude the lower end of the rod so as to be able to protrude and retract, and an inflow path for communicating the storage chamber with the container and an outflow path for communicating with the injection nozzle are provided on the outflow path side. The part is opened when the capsule base and the aqueous solution component in the storage chamber are compressed, and a valve member is provided to allow the capsule base and the aqueous solution component to flow out of the storage chamber. The lower end of the sliding rod that moves is opened when the pressure in the storage chamber is reduced, and a valve member is provided to allow a new capsule base and an aqueous solution component to be sucked in from the container and allowed to flow therein. Emulsified cosmetics and quasi-drugs as claimed in claim having a means for shredding the capsule (1) as it passes through the capsule base that flows out to. 【請求項３】前記カプセルを細断する手段は、前記摺動
杆を上限位置にバネ付勢するために、当該摺動杆の下端
部に上端側を巻装して前記貯留室内に収容させたコイル
スプリングが兼用する請求項（２）に記載した乳化状の
化粧品と医薬部外品。3. A means for shredding the capsule, wherein the upper end side is wound around the lower end portion of the sliding rod so as to bias the sliding rod to the upper limit position, and is accommodated in the storage chamber. The emulsified cosmetics and quasi-drugs according to claim 2, wherein the coil springs are used in combination.
JP2080996A 1990-03-30 1990-03-30 Emulsified cosmetics and quasi-drugs Expired - Lifetime JP2849437B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2080996A JP2849437B2 (en) 1990-03-30 1990-03-30 Emulsified cosmetics and quasi-drugs
FR9103772A FR2660212A1 (en) 1990-03-30 1991-03-28 Process for the preparation of an emulsion and emulsifiable composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2080996A JP2849437B2 (en) 1990-03-30 1990-03-30 Emulsified cosmetics and quasi-drugs

Publications (2)

Publication Number Publication Date
JPH03284607A JPH03284607A (en) 1991-12-16
JP2849437B2 true JP2849437B2 (en) 1999-01-20

Family

ID=13734103

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2080996A Expired - Lifetime JP2849437B2 (en) 1990-03-30 1990-03-30 Emulsified cosmetics and quasi-drugs

Country Status (2)

Country Link
JP (1) JP2849437B2 (en)
FR (1) FR2660212A1 (en)

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US6013270A (en) * 1998-04-20 2000-01-11 The Procter & Gamble Company Skin care kit
FR2786413B1 (en) * 1998-12-01 2001-11-09 Oreal MULTI-PHASE COMPOSITION DELIVERY ASSEMBLY, USE OF SUCH AN ASSEMBLY, AND METHOD OF USE
US6270782B1 (en) * 1999-10-22 2001-08-07 Bath & Body Works, Inc. Body spray composition with pearl-like oil phase droplets in container
DE10232774B4 (en) * 2002-07-18 2004-07-15 Cognis Deutschland Gmbh & Co. Kg Cosmetic preparations with antibacterial properties
JP4305729B2 (en) 2003-03-28 2009-07-29 セイコーエプソン株式会社 Liquid ejecting apparatus and microcapsule manufacturing method
FR2945524B1 (en) * 2009-05-14 2012-11-02 Lrs DEVICE FOR STORING AND RESTITUTING A COSMETIC OR PHARMACEUTICAL FORMULATION CREAM-LIKE PRODUCT
FR2987741B1 (en) * 2012-03-08 2014-04-18 Capsum KIT COMPRISING TWO SEPARATE COMPOSITIONS, IN PARTICULAR FOR A COSMETIC APPLICATION
FR3020052B1 (en) 2014-04-16 2017-03-10 Aptar France Sas FLUID PRODUCT DISPENSER.
DE102015106414A1 (en) * 2015-04-27 2016-10-27 Megaplast Gmbh Dispenser for dispensing liquid to pasty masses
WO2018043661A1 (en) * 2016-09-05 2018-03-08 富士カプセル株式会社 Agar film capsule
FR3067930B1 (en) 2017-06-27 2020-01-10 Capsum DISPERSIONS COMPRISING AT LEAST ONE HYDROCARBON VOLATILE OIL
EP3727281B1 (en) * 2017-12-18 2023-02-22 LVMH Recherche Liquid cosmetic with agar shell capsule
FR3081298B1 (en) 2018-05-23 2022-12-23 Oreal DEVICE FOR PREPARING A COSMETIC COMPOSITION, SET OF CAPSULES AND ASSOCIATED METHOD FOR PREPARING

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Also Published As

Publication number Publication date
JPH03284607A (en) 1991-12-16
FR2660212A1 (en) 1991-10-04

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