JP2008074706A - External preparation for skin - Google Patents

External preparation for skin Download PDF

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JP2008074706A
JP2008074706A JP2006252009A JP2006252009A JP2008074706A JP 2008074706 A JP2008074706 A JP 2008074706A JP 2006252009 A JP2006252009 A JP 2006252009A JP 2006252009 A JP2006252009 A JP 2006252009A JP 2008074706 A JP2008074706 A JP 2008074706A
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external preparation
skin
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JP4974624B2 (en
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Mitsuyo Nozaki
美津世 野崎
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Noevir Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an external preparation for skin, having a characteristic property wherein the external preparation lowers its flowability to change in a gel-like state, when extruded from a pump type container or the like. <P>SOLUTION: This external preparation for skin comprises an acrylic acid-alkyl methacrylate copolymer, one or more surfactants selected from monoalkyl type quaternary ammonium salt type cationic surfactants, and a polyhydric alcohol. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、ポンプ式容器などを用いた場合に、優れた特性を有する皮膚外用剤で、詳しくは、中身を吐出する際のシェアに絡むせん断力によって、流動性が低下し、ゲル状に変化する特異な性質を持った皮膚外用剤に関する。すなわち、シェアが付加される前は、充分な流動性を示すことから、ポンプ式容器などにおいてバルクの吸い込みがスムースでありながら、吐出する際には、ゲル状に変化することから、手にとって肌に適用する時に液ダレを起こしにくいという利点を有するものである。   The present invention is an external preparation for skin having excellent characteristics when using a pump-type container, and more specifically, the fluidity is lowered due to the shear force involved in the shear when discharging the contents, and changes into a gel form. The present invention relates to an external preparation for skin having unique properties. In other words, before the share is added, it exhibits sufficient fluidity, and while sucking in bulk in a pump-type container, etc., it smoothly changes to a gel-like shape when discharged, so it will be skin to the hand. It has the advantage that it does not easily cause dripping when applied to.

本発明は、ポンプ式容器に充填されて用いる場合に、優れた流動性を示し、しかも肌に適用する際にも使用性に優れた皮膚外用剤を得ることを目的とするものである。   An object of the present invention is to obtain an external preparation for skin that exhibits excellent fluidity when used in a pump-type container, and also has excellent usability when applied to the skin.

液状から粘液状の比較的流動性の高い製剤を製品化する場合、ボトル容器や、ポンプ式容器などとの相性は良いが、流動性が高いために、手にとる時や肌に適用する時に、液ダレによって使いにくい場合がある。この場合、コットンなどに予め中身を浸透させるなどして、この欠点をカバーする方法が用いられる。逆にゲル状からクリーム状の流動性の低い製剤を製品化する場合、使用性は良いが、口径の広い容器を用いることになる。すなわち、使用性を考えると、流動性は比較的低い方が好まれ、容器との相性から判断すると、流動性は高いほうが、利便性に優れた容器を採用できる。しかしながら、これらは相反する性質であることから、技術的にも難しく、それ故これを満足させる技術に関する報告はほとんどみられない。このような、作る側と使う側のメリットを活かした製剤技術の開発は課題として常に期待されるが、その報告は少ない。   When commercializing liquid to mucous liquid preparations with relatively high fluidity, compatibility with bottle containers and pump containers is good. , It may be difficult to use due to liquid dripping. In this case, a method of covering this defect by, for example, infiltrating the contents into cotton or the like in advance is used. On the other hand, when a gel-like to cream-like preparation with low fluidity is commercialized, a container having a wide diameter is used although the usability is good. That is, considering the usability, it is preferable that the fluidity is relatively low. Judging from the compatibility with the container, it is possible to adopt a container that is more convenient when the fluidity is higher. However, since these are contradictory properties, they are technically difficult, and therefore there are few reports on techniques that satisfy them. The development of pharmaceutical technology that takes advantage of the advantages of the producer and the user is always expected as a challenge, but there are few reports.

この課題に関する文献として、水溶液状の物性を有し、しかもクリーム状の使用感を備えた水中油型乳化組成物(特許文献1参照)がある。これは、両親媒性物質−界面活性剤−水系にて構成される水中油型乳化組成物に対して、強力な剪断力で処理することにより、これらの性質を示すものである。本文献における組成物は、水溶液状の物性を有し、しかもクリーム状の使用感触を備えた水中油型乳化組成物を提供することを目的としている。本文献発明は、機械的な特殊な処理が必要であり、しかも物性変化は非可逆的現象である。   As a document relating to this problem, there is an oil-in-water emulsion composition (see Patent Document 1) that has an aqueous physical property and has a creamy feeling. This shows these properties by treating the oil-in-water emulsion composition composed of an amphiphile-surfactant-water system with a strong shearing force. The composition in this document is intended to provide an oil-in-water emulsion composition having physical properties in the form of an aqueous solution and having a creamy feel. The invention of this document requires a special mechanical treatment, and the change in physical properties is an irreversible phenomenon.

特開平6−271421公報JP-A-6-271421

本発明においては、ポンプ式容器などとの相性が良く、しかも肌に適用する際にも使用性に優れた皮膚外用剤を提供する方法について鋭意検討した。   In the present invention, a method for providing an external preparation for skin having good compatibility with a pump-type container and the like and having excellent usability even when applied to the skin has been intensively studied.

本発明者は、前記課題を解決するために研究を行った結果、少なくとも(A)アクリル酸・メタクリル酸アルキル共重合体、(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤から選ばれる1種又は2種以上、及び(C)多価アルコールを含有することを特徴とする皮膚外用剤を用いることで、これらの課題を解消できることを見いだし、本発明を完成するに至ったものである。   As a result of researches to solve the above problems, the present inventor has selected at least (A) an acrylic acid / alkyl methacrylate copolymer and (B) a monoalkyl type quaternary ammonium salt type cationic surfactant. It was found that these problems can be solved by using a skin external preparation characterized by containing one or more kinds and (C) a polyhydric alcohol, and the present invention has been completed. is there.

本発明の皮膚外用剤は、静置時には流動性に富んだ粘性液状状態を呈している。これをポンプ式容器などに充填して使用する際、つまり中身が吐出される際には、吐出口部分においてシェアが掛かり、この時流動性が低下して、ゲル状に変化する。   The skin external preparation of the present invention exhibits a viscous liquid state rich in fluidity upon standing. When this is filled in a pump-type container or the like, that is, when the contents are discharged, a share is applied at the discharge port portion, and at this time, the fluidity is lowered to change to a gel state.

すなわち、シェアが付加される前は、充分な流動性を有することから、ポンプ式容器などにおいてバルクの吸い込みがスムースであり、吐出する際は、ゲル状に変化することから、手にとって肌に適用する時に液ダレを起こしにくく使いやすいという、提供する側にとっても、使用する側にとっても、理想的な使用性を達成できる。   That is, before the share is added, it has sufficient fluidity, so bulk suction in a pump type container etc. is smooth, and it changes to a gel when discharging, so it is applied to the skin for the hand In this case, it is possible to achieve ideal usability for both the providing side and the using side, which is less likely to cause dripping and easy to use.

本発明の実施の形態を説明する。   An embodiment of the present invention will be described.

本発明に用いる(A)アクリル酸・メタクリル酸アルキル共重合体は、アクリル酸とメタクリル酸アルキルの共重合体であり、カルボキシル基に起因する親水性部分と、アルキル基に起因する親油性部分とを併せ持ち、良好な乳化性を有した乳化剤としての機能と、増粘剤としての機能を持つ高分子で、ビー・エフ・グッドリッチ(BF Goodrich)社からPEMULEN TR−1,PEMULEN TR−2の商品名で市販されている。これらを使用すると、製剤中に油を乳化することが可能で、あっさりとした使用感が得られる特性がある。アクリル系高分子としては、アルキル変性されていないカルボキシビニルポリマーが、化粧料の増粘剤には一般的に用いられるが、カルボキシビニルポリマーでは、製剤中にモノアルキル型第4級アンモニウム塩型カチオン界面活性剤との凝集体が形成されやすいことから、好ましくない。   The (A) acrylic acid / alkyl methacrylate copolymer used in the present invention is a copolymer of acrylic acid and alkyl methacrylate, and includes a hydrophilic part resulting from a carboxyl group, and a lipophilic part resulting from an alkyl group. It is a polymer with a function as an emulsifier having a good emulsifying property and a function as a thickening agent. From BF Goodrich, PEMULEN TR-1 and PEMULEN TR-2 It is commercially available under the trade name. When these are used, it is possible to emulsify the oil in the preparation, and there is a characteristic that a light usability can be obtained. As the acrylic polymer, a carboxyvinyl polymer which is not alkyl-modified is generally used as a thickener for cosmetics. However, in the case of a carboxyvinyl polymer, a monoalkyl type quaternary ammonium salt type cation is used in the preparation. Since an aggregate with a surfactant is easily formed, it is not preferable.

(A)アクリル酸・メタクリル酸アルキル共重合体の皮膚外用剤への配合量としては、好ましくは、皮膚外用剤全量に対して0.1〜3質量%を用いることができるが、0.1質量%未満では、本発明品の特徴であるシェアによる充分なゲル化現象を起こさず、3質量%を越えると、静止時の状態がゲル状になってしまうことから、本発明の特性を発揮できない。本発明の特性が最も生かされることでは、0.5〜2質量%が特に好ましい。   (A) As a compounding quantity to the skin external preparation of an acrylic acid alkyl methacrylate copolymer, 0.1-3 mass% can preferably be used with respect to the skin external preparation whole quantity, However, 0.1 If it is less than mass%, the gelation phenomenon due to the shear that is a feature of the product of the present invention will not occur, and if it exceeds 3 mass%, the stationary state becomes a gel state, so the characteristics of the present invention are exhibited. Can not. In order to make the most of the characteristics of the present invention, 0.5 to 2% by mass is particularly preferable.

(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤としては、下記一般式(式中、R1は炭素数8〜22のアルキル基またはアルケニル基、R2、R3およびR4は同一又は異なってヒドロキシル基で置換されていてもよい炭素数1〜3のアルキル基またはベンジル基、Xはハロゲン原子を表す)で表されるものを用いることができる。   (B) The monoalkyl type quaternary ammonium salt type cationic surfactant has the following general formula (wherein R1 is an alkyl group or alkenyl group having 8 to 22 carbon atoms, and R2, R3 and R4 are the same or different. An alkyl group having 1 to 3 carbon atoms which may be substituted with a hydroxyl group or a benzyl group, and X represents a halogen atom) can be used.

Figure 2008074706
Figure 2008074706

(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤としては、具体的には、塩化ラウリルトリメチルアンモニウム、塩化ミリスチルトリメチルアンモニウム、塩化セチルトリメチルアンモニウム、塩化ステアリルトリメチルアンモニウム、塩化ベヘニルトリメチルアンモニウム、臭化ラウリルトリメチルアンモニウム、臭化ミリスチルトリメチルアンモニウム、臭化セチルトリメチルアンモニウム、臭化ステアリルトリメチルアンモニウム、臭化ベヘニルトリメチルアンモニウム、塩化ミリスチルジメチルベンジルアンモニウム、塩化セチルジメチルベンジルアンモニウム、塩化オクチルジヒドロキシエチルメチルアンモニウム、塩化2−デシルテトラデシルトリメチルアンモニウム、塩化2−ドデシルヘキサデシルトリメチルアンモニウム等が挙げられる。この中でも、常温下で液状からペースト状の塩化ラウリルトリメチルアンモニウム、塩化ミリスチルトリメチルアンモニウム、塩化セチルトリメチルアンモニウム、塩化ステアリルトリメチルアンモニウムが好ましい。   (B) Specific examples of the monoalkyl type quaternary ammonium salt type cationic surfactant include lauryl trimethyl ammonium chloride, myristyl trimethyl ammonium chloride, cetyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride, behenyl trimethyl ammonium chloride, odor Lauryltrimethylammonium bromide, myristyltrimethylammonium bromide, cetyltrimethylammonium bromide, stearyltrimethylammonium bromide, behenyltrimethylammonium bromide, myristyldimethylbenzylammonium chloride, cetyldimethylbenzylammonium chloride, octyldihydroxyethylmethylammonium chloride, 2 -Decyltetradecyltrimethylammonium chloride, 2-dodecylhexadecyltrimethyl chloride Ammonium and the like. Among these, liquid to paste-like lauryltrimethylammonium chloride, myristyltrimethylammonium chloride, cetyltrimethylammonium chloride, and stearyltrimethylammonium chloride are preferable at room temperature.

(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤の皮膚外用剤への配合量としては、好ましくは、皮膚外用剤全量に対して1〜7質量%を用いることができるが、1質量%未満では、本発明品の特徴であるシェアによる充分なゲル化現象を起こさず、7質量%を越えると、すでにゲル状になってしまい、本発明の特性を発揮できない。本発明の特性が最も生かされることでは、2〜6質量%が特に好ましい。   (B) As a compounding quantity to the skin external preparation of a monoalkyl type | mold quaternary ammonium salt type cationic surfactant, Preferably 1-7 mass% can be used with respect to the skin external preparation whole quantity, but 1 If it is less than mass%, the sufficient gelation phenomenon due to the shear, which is a feature of the product of the present invention, does not occur, and if it exceeds 7 mass%, it already becomes a gel and cannot exhibit the characteristics of the present invention. In order to make the most of the characteristics of the present invention, 2 to 6% by mass is particularly preferable.

さらに(A)アクリル酸・メタクリル酸アルキル共重合体と(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤の配合比率としては、質量比で1:1〜1:4であることが好ましい。この配合比を外れると、本発明品の特徴であるシェアによるゲル化現象が生じない。   Further, the blending ratio of (A) acrylic acid / alkyl methacrylate copolymer and (B) monoalkyl type quaternary ammonium salt type cationic surfactant is 1: 1 to 1: 4 in mass ratio. preferable. If this blending ratio is deviated, the gelation phenomenon due to the shear, which is a feature of the product of the present invention, does not occur.

(C)多価アルコールとしては、グリセリン、1,3−ブチレングリコール、ジグリセリン、ジプロピレングリコールから選ばれる1種または2種以上を用いることができる。   (C) As a polyhydric alcohol, 1 type, or 2 or more types chosen from glycerol, 1, 3- butylene glycol, diglycerol, and a dipropylene glycol can be used.

(C)多価アルコールの皮膚外用剤への配合量としては、好ましくは、皮膚外用剤全量に対して8〜45質量%を用いることができる。8質量%未満では、製剤中に凝集物が発生しやすく、状態も不安定である。特に10℃以下の低温時に、顕著に白く濁ってしまうことがある。45質量%を越えると、べたつきが顕著に現われ、肌に違和感や不快感を感じてしまう。10〜40質量%が特に好ましい。   (C) As a compounding quantity to the skin external preparation of a polyhydric alcohol, Preferably, 8-45 mass% can be used with respect to the skin external preparation whole quantity. If the amount is less than 8% by mass, aggregates are easily generated in the preparation, and the state is unstable. In particular, at a low temperature of 10 ° C. or less, it may become significantly white and cloudy. If it exceeds 45% by mass, stickiness appears remarkably and the skin feels uncomfortable and uncomfortable. 10-40 mass% is especially preferable.

本発明の皮膚外用剤は、(A)(B)(C)以外の成分が、流動性に影響しない範囲であれば、ブルックフィールド型回転粘度計(例えば(株)東京精機製作所製粘度計)を用いて測定温度25℃、ローター番号4番、回転速度6rpmにて測定した粘度は、25000mPa・s以下である。本発明の皮膚外用剤は、強いせん断力が負荷されるほど、ゲル構造の形成が促進され、粘度の上昇が観測される。皮膚外用剤に用いられるポンプ式容器は、一般に、内口径0.3〜1.5mmのものが用いられる。このポンプ式容器吐出口から吐出された直後の粘度は、静置時と同条件で測定した場合、30000〜60000mPa・sであり、明らかな上昇が観察される。しかも、この現象は可逆的であり、しばらく静置すると当初の流動性に戻るという特性がある。このような特性を示すことから、容器に充填する段階や製造時などに、大きなせん断力が負荷されてゲル構造が形成されたとしても、静置しておくことで当初の物性に戻ることから、このことによる問題は発生しないのも利点である。   The skin external preparation of the present invention has a Brookfield rotational viscometer (for example, a viscometer manufactured by Tokyo Seiki Seisakusho Co., Ltd.) as long as components other than (A), (B), and (C) do not affect fluidity. The viscosity measured at a measurement temperature of 25 ° C., a rotor number of 4 and a rotational speed of 6 rpm is 25000 mPa · s or less. In the external preparation for skin of the present invention, the formation of a gel structure is promoted and an increase in viscosity is observed as a stronger shearing force is applied. The pump type container used for the external preparation for skin is generally used with an inner diameter of 0.3 to 1.5 mm. The viscosity immediately after being discharged from the pump-type container discharge port is 30000 to 60000 mPa · s when measured under the same conditions as when standing, and a clear increase is observed. In addition, this phenomenon is reversible and has the property of returning to the original fluidity after standing for a while. Because it shows such characteristics, even when a gel structure is formed by applying a large shear force during the filling of the container or at the time of manufacture, it returns to the original physical properties by leaving it still. It is also an advantage that the problem caused by this does not occur.

本発明の皮膚外用剤には、必須成分としての(A)アクリル酸・メタクリル酸アルキル共重合体、(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤、(C)多価アルコールのほかに、本発明品の効果を損なわない範囲で、一般的な化粧料や医薬部外品に配合される他の成分、例えば油脂,界面活性剤,保湿剤,無機粉体,有機粉体,紫外線吸収剤,pH調整剤,キレート剤,薬剤,香料,樹脂,その他アルコール類などを、適宜必要に応じて配合することができる。   The skin external preparation of the present invention includes (A) an acrylic acid / alkyl methacrylate copolymer as an essential component, (B) a monoalkyl type quaternary ammonium salt type cationic surfactant, and (C) a polyhydric alcohol. In addition, other ingredients blended in general cosmetics and quasi-drugs, such as fats and oils, surfactants, moisturizers, inorganic powders, organic powders, as long as the effects of the present invention are not impaired. An ultraviolet absorber, a pH adjuster, a chelating agent, a drug, a fragrance, a resin, and other alcohols can be appropriately blended as necessary.

また、本発明の皮膚外用剤は、(C)多価アルコールに対し(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤を均一に混合溶解させた後、(A)アクリル酸・メタクリル酸アルキル共重合体の水溶液を加えることにより製造するのが好ましい。(B)に(A)を直接作用させると、相互作用により凝集物が形成されやすい傾向がみられる。   The external preparation for skin of the present invention comprises (B) a monoalkyl type quaternary ammonium salt type cationic surfactant that is uniformly mixed and dissolved in (C) polyhydric alcohol, and then (A) acrylic acid / methacrylic acid. It is preferably produced by adding an aqueous solution of an acid alkyl copolymer. When (A) is allowed to act directly on (B), there is a tendency that aggregates are easily formed by the interaction.

次に本発明を実施例によりさらに詳しく説明するが、本発明の皮膚外用剤は、これらに限定されるものではない。   EXAMPLES Next, although an Example demonstrates this invention further in detail, the skin external preparation of this invention is not limited to these.

表1に本発明の実施例、およびその比較として比較例1〜3を示す。また、表2にその評価結果を示す。   Table 1 shows examples of the present invention and comparative examples 1 to 3 as a comparison. Table 2 shows the evaluation results.

Figure 2008074706
Figure 2008074706

製造方法:
成分3を4の精製水に溶解する。成分1〜2を混合加熱溶解した後、予め調製した成分3〜4の水溶液を加え、混合均一化する。
Production method:
Dissolve component 3 in 4 purified water. After components 1 and 2 are mixed and dissolved by heating, an aqueous solution of components 3 and 4 prepared in advance is added to mix and homogenize.

Figure 2008074706
Figure 2008074706

以上の結果より、比較例においては、本発明の特性を呈しないことが確認された。   From the above results, it was confirmed that the comparative example does not exhibit the characteristics of the present invention.

次に実施例1の皮膚外用剤について、せん断試験を行った。内口径0.3mm、0.9mmおよび1.5mmのポンプ容器を準備し、吐出前と吐出後の粘度変化を測定した。粘度は、株式会社東京精機製作所製ブルックフィールド型回転粘度計を用いて、測定温度25℃、ローター番号4番、回転速度6rpmでの粘度を測定した。本発明におけるゲル化現象は、可逆的であることから、吐出後即座に測定した。静置5分後の粘度についても測定した。結果を表3に示す。   Next, the skin external preparation of Example 1 was subjected to a shear test. Pump containers having inner diameters of 0.3 mm, 0.9 mm, and 1.5 mm were prepared, and changes in viscosity before and after discharge were measured. The viscosity was measured using a Brookfield rotary viscometer manufactured by Tokyo Seiki Seisakusho Co., Ltd. at a measurement temperature of 25 ° C., a rotor number of 4 and a rotational speed of 6 rpm. Since the gelation phenomenon in the present invention is reversible, it was measured immediately after ejection. The viscosity after 5 minutes of standing was also measured. The results are shown in Table 3.

Figure 2008074706
Figure 2008074706

以上の結果からも、本発明の特性が確認できた。また、強いせん断が負荷されるほど、粘度の上昇が観察された。また、静置後は、元の物性にもどることも確認された。   From the above results, the characteristics of the present invention could be confirmed. In addition, an increase in viscosity was observed as the strong shear was applied. It was also confirmed that the properties returned to their original properties after standing.

以下、その他本発明の実施例を記載する。   Hereinafter, other examples of the present invention will be described.

[実施例2]ジェル状化粧料
1.グリセリン 25.0(質量%)
2.塩化ステアリルトリメチルアンモニウム 4.0
3.アクリル酸・メタクリル酸アルキル共重合体 1.4
4.精製水 69.0
5.エタノール 0.4
6.パラオキシ安息香酸メチル 0.1
7.香料 0.1
製造方法:
成分3を成分4の精製水に溶解する。成分1〜2を混合加熱溶解した後、予め調製した成分3〜4の水溶液を加え混合均一化し、成分5〜7を加える。
[Example 2] Gel cosmetic 1. Glycerin 25.0 (mass%)
2. Stearyltrimethylammonium chloride 4.0
3. Acrylic acid / alkyl methacrylate copolymer 1.4
4). Purified water 69.0
5. Ethanol 0.4
6). Methyl paraoxybenzoate 0.1
7). Fragrance 0.1
Production method:
Ingredient 3 is dissolved in purified water of ingredient 4. After components 1 and 2 are mixed and heated and dissolved, an aqueous solution of components 3 to 4 prepared in advance is added to mix and homogenize, and components 5 to 7 are added.

[実施例3]ジェル状化粧料
1.1,3ブチレングリコール 10.0(質量%)
2.グリセリン 15.0
3.塩化セチルトリメチルアンモニウム 1.0
4.塩化ステアリルトリメチルアンモニウム 3.0
5.アクリル酸・メタクリル酸アルキル共重合体 1.5
6.精製水 68.9
7.エタノール 0.4
8.パラオキシ安息香酸メチル 0.1
9.香料 0.1
製造方法:
成分5を成分6の精製水に溶解する。成分1〜4を混合加熱溶解した後、予め調製した成分5〜6の水溶液を加え混合均一化し、成分7〜9を加える。
[Example 3] Gel cosmetic 1.1,3 butylene glycol 10.0 (mass%)
2. Glycerin 15.0
3. Cetyltrimethylammonium chloride 1.0
4). Stearyltrimethylammonium chloride 3.0
5. Acrylic acid / alkyl methacrylate copolymer 1.5
6). Purified water 68.9
7). Ethanol 0.4
8). Methyl paraoxybenzoate 0.1
9. Fragrance 0.1
Production method:
Ingredient 5 is dissolved in purified water of ingredient 6. After components 1 to 4 are mixed and dissolved by heating, an aqueous solution of components 5 to 6 prepared in advance is added and mixed, and components 7 to 9 are added.

[実施例4]ジェル状化粧料
1.ジグリセリン 5.0(質量%)
2.グリセリン 10.0
3.塩化ステアリルトリメチルアンモニウム 3.0
4.アクリル酸・メタクリル酸アルキル共重合体 1.2
5.精製水 80.2
6.エタノール 0.4
7.パラオキシ安息香酸メチル 0.1
8.香料 0.1
製造方法:
成分4を成分5の精製水に溶解する。成分1〜3を混合加熱溶解した後、予め調製した成分4〜5の水溶液を加え混合均一化し、成分6〜8を加える。
[Example 4] Gel cosmetic 1. Diglycerin 5.0 (mass%)
2. Glycerin 10.0
3. Stearyltrimethylammonium chloride 3.0
4). Acrylic acid / alkyl methacrylate copolymer 1.2
5. Purified water 80.2
6). Ethanol 0.4
7). Methyl paraoxybenzoate 0.1
8). Fragrance 0.1
Production method:
Ingredient 4 is dissolved in purified water of ingredient 5. After components 1 to 3 are mixed and dissolved by heating, an aqueous solution of components 4 to 5 prepared in advance is added to mix and homogenize, and components 6 to 8 are added.

本発明の皮膚外用剤は、以上の実施例2〜4においても、本発明の特性であるシェアが掛かることによるゲル化現象を示すことが確認された。   It was confirmed that the skin external preparation of the present invention also exhibits a gelation phenomenon due to the application of the shear, which is a characteristic of the present invention, in Examples 2 to 4 described above.

Claims (5)

ポンプ式容器に充填された時の粘度が25000mPa・s以下の組成物であって、ポンプ式容器吐出口から吐出される際のせん断力により、その直後の粘度が30000〜60000mPa・sを示すことを特徴とする皮膚外用剤。 It is a composition having a viscosity of 25000 mPa · s or less when filled in a pump-type container, and the viscosity immediately after that shows a viscosity of 30000-60000 mPa · s due to the shearing force when discharged from the pump-type container discharge port. An external preparation for skin. 少なくとも(A)、(B)及び(C)を含有することを特徴とする請求項1記載の皮膚外用剤。
(A)アクリル酸・メタクリル酸アルキル共重合体
(B)モノアルキル型第4級アンモニウム塩型カチオン界面活性剤から選ばれる1種又は2種以上
(C)多価アルコール
The skin external preparation according to claim 1, comprising at least (A), (B) and (C).
(A) Acrylic acid / alkyl methacrylate copolymer (B) One or more selected from monoalkyl type quaternary ammonium salt type cationic surfactants (C) Polyhydric alcohol
前記成分(A)、(B)及び(C)を、(A)0.5〜2質量%、(B)2〜6質量%、(C)10〜40質量%含有し、(A)と(B)の配合比率が質量比で1:1〜1:4であることを特徴とする請求項1又は2記載の皮膚外用剤。 (A) 0.5-2 mass%, (B) 2-6 mass%, (C) 10-40 mass% containing the said component (A), (B) and (C), (A) and The external preparation for skin according to claim 1 or 2, wherein the blending ratio of (B) is 1: 1 to 1: 4 by mass ratio. (C)多価アルコールが、グリセリン、1,3−ブチレングリコール、ジグリセリン、ジプロピレングリコールから選ばれる1種または2種以上である請求項1〜3の1項に記載の皮膚外用剤。 (C) The external preparation for skin according to any one of claims 1 to 3, wherein the polyhydric alcohol is one or more selected from glycerin, 1,3-butylene glycol, diglycerin and dipropylene glycol. (C)成分に対し(B)成分を均一に混合溶解させた後、(A)成分の水溶液を加えて混合することを特徴とする請求項1〜4の1項に記載の皮膚外用剤の製造方法。 The skin external preparation according to claim 1, wherein the component (B) is uniformly mixed and dissolved in the component (C), and then the aqueous solution of the component (A) is added and mixed. Production method.
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Publication number Priority date Publication date Assignee Title
US8668916B2 (en) 2010-09-24 2014-03-11 Conopco, Inc. HIPE-gelation process for making highly concentrated, spherical biopolymer gel particle suspensions
JP2017124980A (en) * 2016-01-13 2017-07-20 ホーユー株式会社 Hair cosmetic, method for dying, destaining or bleaching hair
JP2019104765A (en) * 2019-04-05 2019-06-27 株式会社ダリヤ Two-agent simultaneous discharge type hair dye
JP2021100980A (en) * 2015-12-28 2021-07-08 花王株式会社 Second agent composition of aerosol type hair dyeing or hair decolorizing agent

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JPH11199454A (en) * 1998-01-08 1999-07-27 Yamahatsu Sangyo Kk Two-pack type oxidation hair dye and two-pack type decoloring agent
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JP2007277117A (en) * 2006-04-04 2007-10-25 Kao Corp Dilatancy composition

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JPH08291029A (en) * 1995-04-18 1996-11-05 Hoyu Co Ltd Straight permanent wave agent
JPH11199454A (en) * 1998-01-08 1999-07-27 Yamahatsu Sangyo Kk Two-pack type oxidation hair dye and two-pack type decoloring agent
JP2002317124A (en) * 2001-04-18 2002-10-31 Kao Corp Dilatancy composition
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8668916B2 (en) 2010-09-24 2014-03-11 Conopco, Inc. HIPE-gelation process for making highly concentrated, spherical biopolymer gel particle suspensions
JP2021100980A (en) * 2015-12-28 2021-07-08 花王株式会社 Second agent composition of aerosol type hair dyeing or hair decolorizing agent
JP7274519B2 (en) 2015-12-28 2023-05-16 花王株式会社 Second agent composition for aerosol type hair dye or hair bleaching agent
JP2017124980A (en) * 2016-01-13 2017-07-20 ホーユー株式会社 Hair cosmetic, method for dying, destaining or bleaching hair
JP2019104765A (en) * 2019-04-05 2019-06-27 株式会社ダリヤ Two-agent simultaneous discharge type hair dye

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