JPH0393709A - Pack agent for film forming type make-up - Google Patents
Pack agent for film forming type make-upInfo
- Publication number
- JPH0393709A JPH0393709A JP22933289A JP22933289A JPH0393709A JP H0393709 A JPH0393709 A JP H0393709A JP 22933289 A JP22933289 A JP 22933289A JP 22933289 A JP22933289 A JP 22933289A JP H0393709 A JPH0393709 A JP H0393709A
- Authority
- JP
- Japan
- Prior art keywords
- agent
- weight
- pack
- film
- forming
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 63
- -1 polyethylene octyl dodecyl ether Polymers 0.000 claims abstract description 22
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000002537 cosmetic Substances 0.000 claims description 16
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract description 6
- 238000001035 drying Methods 0.000 abstract description 3
- 239000007864 aqueous solution Substances 0.000 abstract description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 abstract description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 abstract description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 abstract description 2
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 239000000499 gel Substances 0.000 description 8
- 229940079593 drug Drugs 0.000 description 7
- 239000003814 drug Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 210000003491 skin Anatomy 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 239000008213 purified water Substances 0.000 description 6
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 108010006161 conchiolin Proteins 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 150000005846 sugar alcohols Polymers 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000003755 preservative agent Substances 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000003020 moisturizing effect Effects 0.000 description 3
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 3
- 230000002335 preservative effect Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 229940032094 squalane Drugs 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- BGRXBNZMPMGLQI-UHFFFAOYSA-N 2-octyldodecyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(CCCCCCCC)CCCCCCCCCC BGRXBNZMPMGLQI-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 229940073665 octyldodecyl myristate Drugs 0.000 description 2
- 239000004006 olive oil Substances 0.000 description 2
- 235000008390 olive oil Nutrition 0.000 description 2
- 210000002826 placenta Anatomy 0.000 description 2
- 229920000223 polyglycerol Polymers 0.000 description 2
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 150000003700 vitamin C derivatives Chemical class 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- DGSZGZSCHSQXFV-UHFFFAOYSA-N 2,3-bis(2-ethylhexanoyloxy)propyl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OCC(OC(=O)C(CC)CCCC)COC(=O)C(CC)CCCC DGSZGZSCHSQXFV-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000384508 Hoplostethus atlanticus Species 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000270666 Testudines Species 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 229940069521 aloe extract Drugs 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- FCQAMVZGVMHDFT-UHFFFAOYSA-N butane-1,4-diol;propane-1,2,3-triol Chemical compound OCCCCO.OCC(O)CO FCQAMVZGVMHDFT-UHFFFAOYSA-N 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- 229940105990 diglycerin Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229940113120 dipropylene glycol Drugs 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229940119170 jojoba wax Drugs 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229940109850 royal jelly Drugs 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、化粧用バック剤に関する。更に詳細には二剤
型皮膜形成型化粧用パック剤に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a cosmetic backing agent. More specifically, the present invention relates to a two-part film-forming cosmetic pack.
乾燥後に皮膜を形威しないタイプのパック剤もあるが、
これにくらべて、皮膜形成型バック剤は、皮膚面から蒸
散する水分をパックの遮蔽効果によって、バック層の下
にとどまらせ、もって表面角質層を柔軟化させると共に
、皮孔を拡げ、その結果バック中の有効成分が容易に皮
膚内に浸透することができるので、パック本来の効果が
強く発揮される。したがって、現在パック剤としては、
このような皮膜形成型のバック剤が多用されている。There are also types of packs that do not leave a film after drying, but
In comparison, film-forming backing agents allow moisture that evaporates from the skin surface to stay under the backing layer due to the shielding effect of the pack, softening the surface stratum corneum and expanding the skin pores, resulting in Since the active ingredients in the bag can easily penetrate into the skin, the pack's original effects are strongly demonstrated. Therefore, currently as a pack agent,
Such film-forming backing agents are often used.
しかしながら、これら既知のバック剤は、皮膚より剥離
する時に痛い、しっとり感が弱い、乾燥したかどうかの
確認が困難、油剤の浮上等の分離現象が生じ易い等のい
くつかの欠点を有していたが、本出願人による特開昭6
3−57508号公報によって、これらの問題を解決し
た2剤型のバック剤が提案された。However, these known backing agents have several drawbacks, such as being painful when peeled off from the skin, having a weak moisturizing sensation, making it difficult to confirm whether or not they have dried, and easily causing separation phenomena such as floating of oil. However, the applicant's Japanese Patent Application Laid-open No. 6
No. 3-57508 proposed a two-pack type backing agent that solved these problems.
これらの皮膜形成型のバック剤の問題は一応解決された
が、なお第1剤のゲルののびが悪く、また透明感も悪い
ことから更に一層の改良が望まれていた。Although the problems of these film-forming backing agents have been solved to some extent, further improvements have been desired since the gel of the first agent does not spread well and has poor transparency.
本発明の目的は、従来の2剤型の化粧用皮膜形成型バッ
ク剤の欠点である、のびと透明感を改良し、のびが良好
であり、透明感も優れ、なおしつとり感においても優れ
た化粧用皮膜形成型バック剤を提供することである。The purpose of the present invention is to improve spreadability and transparency, which are the drawbacks of conventional two-component cosmetic film-forming backing agents, and to achieve good spreadability, excellent transparency, and excellent dewy feeling. An object of the present invention is to provide a cosmetic film-forming backing agent.
本発明者らは、前記の課題を解決するため、各種原料に
ついて鋭意研究を行った結果、ポリグリセリン脂肪酸エ
ステルより優れた原料としてポリオキシエチレンオクチ
ルドデシルエーテルが前記目的に合致することを見い出
し本発明を完成した。In order to solve the above-mentioned problems, the present inventors conducted intensive research on various raw materials and found that polyoxyethylene octyl dodecyl ether met the above-mentioned purpose as a raw material superior to polyglycerin fatty acid ester. completed.
すなわち本発明はエチレンオキサイドの重合モル数10
〜100のポリオキシエチレンオクチルドデシルエーテ
ルを含有する第一剤と、皮膜形或剤を含有する第二剤と
から成る皮膜形成型化粧用バック剤である。That is, in the present invention, the number of polymerized moles of ethylene oxide is 10.
This is a film-forming cosmetic backing agent consisting of a first part containing polyoxyethylene octyl dodecyl ether of ~100 and a second part containing a film-forming agent.
エチレンオキサイドの重合モル数としては、10〜50
が更に好ましい。重合モル数の同一なポリオキシエチレ
ンオクチルドデシルエーテル単独でもよく、又重合モル
数の異なる原料を組み合わせて用いてもよいが、他の原
料との組み合わせを考慮して選択する必要がある。The number of polymerized moles of ethylene oxide is 10 to 50
is even more preferable. Polyoxyethylene octyl dodecyl ether having the same number of polymerized moles may be used alone, or raw materials having different numbers of polymerized moles may be used in combination, but it is necessary to select it in consideration of the combination with other raw materials.
ポリグリセリン脂肪酸エステルを、このポリオキシエチ
レンオクチルドデシルエーテルと併用することもなんら
問題はないが、ポリグリセリン脂肪酸エステルの量を余
り多くすれば、本発明の利点を活かせないことはいうま
でもない。Although there is no problem in using polyglycerol fatty acid ester in combination with this polyoxyethylene octyl dodecyl ether, it goes without saying that if the amount of polyglycerol fatty acid ester is too large, the advantages of the present invention cannot be utilized.
第1剤の透明ゲルは、ポリオキシエチレンオクチルドデ
シルエーテルのほか、油剤及び多価アルコールから威る
ものであるが、油剤としては化粧品に使用される固体状
、ペースト状ないし液体状の化粧用油剤が、すべて使用
できる。例えば、化粧用液体状油剤としては、スクヮラ
ン、流動バラフィン、プリスタンなどの化粧用液状炭化
水素類;ミリスチン酸オクチルドデシル、ミリスチン酸
イソブロビル、ワシノレイン酸オクチルドデシルなどの
化粧用液状エステル;ヤシ油、ホホバ油、オリーブ油、
アルモンド油、タートル油、オレンジラッフィー油など
の化粧用液状動植物油;カプリルカプロン酸トリグリセ
ライドなどの化粧用液状トリグリセライド、これらの単
独或いは2種以上の混合物が挙げられる。The first agent, the transparent gel, is made from polyoxyethylene octyl dodecyl ether, as well as oils and polyhydric alcohols.The oils include solid, paste, or liquid cosmetic oils used in cosmetics. But all can be used. For example, cosmetic liquid oil agents include cosmetic liquid hydrocarbons such as squalane, liquid paraffin, and pristane; cosmetic liquid esters such as octyldodecyl myristate, isobrobyl myristate, and octyldodecyl wasinolate; coconut oil, and jojoba oil. ,olive oil,
Cosmetic liquid animal and vegetable oils such as almond oil, turtle oil, and orange roughy oil; cosmetic liquid triglycerides such as caprylic caproic acid triglyceride; these may be used alone or in mixtures of two or more thereof.
ただ、固体或いはペースト状油剤も利用できるが、油剤
全部をこれに置き換えるとゲルの硬さが高すぎて、使用
にたえないのは当然である。However, solid or paste-like oils can also be used, but if all the oils are replaced with these, the hardness of the gel will be too high to be useful.
また油剤は単一の原料を用いるよりも、炭化水素系のも
のと、トリグリセライドを組み合わせた方がよりよいゲ
ルが形成される。In addition, a better gel is formed by combining a hydrocarbon-based oil and a triglyceride than by using a single raw material.
多価アルコールは、グリセリン、1,3ブチレングリコ
ール、プロピレングリコール、ジグリセリン、ジプロピ
レングリコール、ポリエチレングリコール(分子量が2
00〜600)等のほかにソルビトール、マルピット等
も利用できる。Polyhydric alcohols include glycerin, 1,3 butylene glycol, propylene glycol, diglycerin, dipropylene glycol, polyethylene glycol (with a molecular weight of 2
00 to 600), sorbitol, Marpit, etc. can also be used.
しかしながらグリセリンが一番ゲル形成がよい。However, glycerin forms the best gel.
多価アルコールは、単用しても或いは2種以上併用して
もよいことは当然である。It goes without saying that polyhydric alcohols may be used alone or in combination of two or more.
更に、水を添加する場合には、油剤の種類及び使用量に
もよるが、一般的には約10〜20重量%以上使用する
と、ゲル性または透明性が損なわれるので注意を要する
。ゲル化に好適な水分量は約0.5〜8重量%であり、
更に好ましい水分量は約2〜5重量%である。Furthermore, when adding water, care must be taken, since gelling properties or transparency will be impaired if water is added in an amount of about 10 to 20% by weight or more, although it depends on the type of oil agent and the amount used. The water content suitable for gelation is about 0.5 to 8% by weight,
A more preferred water content is about 2-5% by weight.
これらに加えて、ビタミンE1ビタミンA1ジパルミチ
ン酸等油溶性薬剤を添加すると、バック剤としての効果
を更に高めることができる。In addition to these, the effect as a backing agent can be further enhanced by adding oil-soluble drugs such as vitamin E, vitamin A, and dipalmitic acid.
第一剤を調製するには、常法によって、薬剤の種類によ
り加温が必要なものは加温し、溶融ないし流動性を高め
ながら他の薬剤を加えて充分に混合し、冷却すればよく
、このようにして透明なゲルが得られる。各薬剤の混合
比率は、例えば次のとおりである。To prepare the first agent, use the conventional method to heat drugs that require heating depending on the type of drug, add other drugs to increase melting or fluidity, mix thoroughly, and cool. , thus a transparent gel is obtained. The mixing ratio of each drug is, for example, as follows.
ポリオキシエチレンオクチルドデシルエーテル2〜30
重量%、好ましくは5〜15重量%;多価アルコール0
.5〜40重量%、好ましくは5〜25重量%;化粧用
油脂20〜95重量%、好ましくは50〜80重量%;
水20重量%以下。Polyoxyethylene octyl dodecyl ether 2-30
% by weight, preferably 5-15% by weight; 0 polyhydric alcohols
.. 5-40% by weight, preferably 5-25% by weight; cosmetic oils and fats 20-95% by weight, preferably 50-80% by weight;
Water 20% by weight or less.
混合比率は、通常は上記範囲内で適宜選択するが、必要
ある場合には上記範囲に限定されることなく、必要な混
合比率を採ってもよい。The mixing ratio is usually appropriately selected within the above range, but if necessary, a necessary mixing ratio may be adopted without being limited to the above range.
第二剤は皮膜形或剤の水溶液であり、皮膜形成剤として
は、ポリビニルアルコール、ポリビニルピロリドン、カ
ルボキシビニルモノマー カルボキシメチルセルロース
その他が単用または併用できる。The second agent is an aqueous solution of a film-forming agent, and polyvinyl alcohol, polyvinylpyrrolidone, carboxyvinyl monomer carboxymethylcellulose, and others can be used alone or in combination as the film-forming agent.
皮膜形成剤の含有量は0.5〜50重量%、好ましくは
2〜30重量%である。The content of the film forming agent is 0.5 to 50% by weight, preferably 2 to 30% by weight.
第二剤には更に、水溶性薬剤、エタノール、多価アルコ
ール、防腐剤等を適宜添加することも可能である。It is also possible to further appropriately add water-soluble drugs, ethanol, polyhydric alcohols, preservatives, etc. to the second agent.
水溶性薬剤としては、ビタミンC1その誘導体、アロエ
エキス、ローヤルゼリー、ブラセンタエキス、蜂蜜、黒
糖、その他動植物成分、コンキオリン加水分解物等が例
示される。Examples of water-soluble drugs include vitamin C1 derivatives, aloe extract, royal jelly, placenta extract, honey, brown sugar, other animal and plant components, and conchiolin hydrolyzate.
コンキオリン加水分解物とは、コンキオリンの加水分解
物すべてを指すが、例えば、コンキオリンを塩酸分解し
た後、塩酸を除去し、次いで限外濾過したり、或いはコ
ンキオリンを硫酸分解した後、強酸性pHとなるよう第
1段の中和を行い、次いで中性付近の弱酸性pHとなる
ように第2段の中和を行い、そして生成した沈澱物を除
去してなるものであって、皮膚のカプレや発赤の原因と
なる高分子ペプタイドを除去してなる極めて安全な整肌
効果のすぐれた化粧品原料である。Conchiolin hydrolyzate refers to all hydrolysates of conchiolin, but for example, conchiolin is decomposed with hydrochloric acid, the hydrochloric acid is removed, and then ultrafiltrated, or conchiolin is decomposed with sulfuric acid and then treated with strong acidic pH. The first stage of neutralization is carried out so that the pH is slightly acidic, and then the second stage of neutralization is carried out so that the pH becomes slightly acidic near neutral, and the generated precipitate is removed. It is an extremely safe cosmetic ingredient that has excellent skin conditioning effects and is made by removing polymeric peptides that cause redness.
本発明にかかわるパック剤は、透明ゲルからなる第一剤
と、透明皮膜形成剤からなる第二剤とから構威される新
規な2威分系のバック剤である。The pack agent according to the present invention is a novel two-part backing agent composed of a first agent consisting of a transparent gel and a second agent consisting of a transparent film forming agent.
使用に当っては、まず第一剤を皮膚表面に塗布し、続い
て第二剤をその上に塗布し、乾燥して必要時間経過後に
剥離すればよい。In use, first the first agent is applied to the skin surface, then the second agent is applied thereon, dried, and peeled off after a required period of time.
第二剤を塗布した時、二つの液が混合されて白濁し、乾
燥すると透明になり、したがって剥離時期が明確になる
。When the second agent is applied, the two liquids are mixed and become cloudy, and when dry, they become transparent, which makes it clear when it is time to peel them off.
また第二剤を塗布した後も、第一剤が皮膚上に薄い皮膜
を形成しており、したがって、しっとり感が向上すると
共に、これを剥離する時に・刺激がなくなり、剥離時の
いたみがなくなる。In addition, even after applying the second agent, the first agent forms a thin film on the skin, which improves the moisturizing feeling and eliminates irritation and pain when peeling off. .
またバック剤を2成分系に分離したために、油剤の浮上
等の分離現象が防止される。Furthermore, since the backing agent is separated into a two-component system, separation phenomena such as floating of the oil agent are prevented.
このような2剤型パック剤の効果に加えて、本発明のパ
ック剤では、のびが格段に良好になり、透明感も大巾に
改善される。またしっとり感もより良好になる。In addition to the effects of the two-component pack agent, the pack agent of the present invention spreads much better and the transparency is also greatly improved. Also, the moist feeling becomes better.
以下に実施例によって、本発明を更に具体的に説明する
が、本発明はこの実施例によって何等限定されるもので
はない。EXAMPLES The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to these Examples in any way.
(実施例1)
第一剤
A)ボリオキシエチレンオクチルドデシルエーテル(2
0E.0.) 1 0重量%グリセ
リン 15重量%B)スクワ
ラン 50重量%カプリルカ
ブロン酸トリグリセライド 20重量%精製水
5重量%A)を加温溶解し、
B)を撹はんしつつゆっくり加えて冷却する。(Example 1) First agent A) polyoxyethylene octyl dodecyl ether (2
0E. 0. ) 1 0% by weight Glycerin 15% by weight B) Squalane 50% by weight Caprycabroic acid triglyceride 20% by weight Purified water
5% by weight A) was dissolved by heating,
Add B) slowly while stirring and cool.
第二剤
ポリビニルアルコール 15重量%グリ
セリン 5重量%エタノー
ル 5重量%防腐剤
適 量ビタミンC誘導体
適 量精製水
(実施例2)
第一剤
A)ポリオキシエチレンオクチルドデシルエーテル(5
E.O.)
ボリオキシエチレンオクチルドデシル
エーテル(50E.0.)
1.3ブチレングリコール
グリセリン
B)流動バラフィン
ミリスチン酸オクチルドデジル
精製水
A)を加温溶解し、
り加えて冷却する。Second component Polyvinyl alcohol 15% by weight Glycerin 5% by weight Ethanol 5% by weight Preservative
Appropriate amount of vitamin C derivative
Appropriate amount of purified water (Example 2) First agent A) Polyoxyethylene octyl dodecyl ether (5
E. O. ) Polyoxyethylene octyl dodecyl ether (50E.0.) 1.3 Butylene glycol glycerin B) Liquid paraffin octyl dodecyl myristate Dissolve purified water A) by heating, add and cool.
第二剤
ポリビニルアルコール
酢酸ビニルエマルジョン
PEGIOOO
エタノール
防腐剤
10重量%
5重量%
15重量%
45重量%
15重量%
5重量%
B)を撹はんしっつゆっく
75重量%
5重量%
12重量%
10重量%
5重量%
5重量%
適量
ビタミンC誘導体 適 量ブラセ
ンターエキス 適 量精製水
68重量%(実施例3)
第一剤
A)ポリオキシエチレンオクチルドデシルエーテル(
1 5E.0.) 12重量%グリセ
リン 15重量%プロピレン
グリコール 5重量%B)スクワラン
50重量%オリーブ油
6重量%2エチルへキサン酸
トリグリセライド 7重量%精製水 ′
5重量%A)を加温溶解し、B)を
撹はんしつつゆっくり加えて冷却する。Second Part Polyvinyl Alcohol Vinyl Acetate Emulsion PEGIOOO Ethanol Preservative 10% by weight 5% by weight 15% by weight 45% by weight 15% by weight 5% by weight Stir B) slowly 75% by weight 5% by weight 12% by weight 10% by weight 5% by weight 5% by weight Appropriate amount Vitamin C derivative Appropriate amount Bra center extract Appropriate amount Purified water
68% by weight (Example 3) First agent A) Polyoxyethylene octyl dodecyl ether (
1 5E. 0. ) 12% by weight Glycerin 15% by weight Propylene glycol 5% by weight B) Squalane 50% by weight Olive oil
6% by weight 2-ethylhexanoic acid triglyceride 7% by weight purified water'
5% by weight of A) is dissolved by heating, B) is slowly added while stirring, and the mixture is cooled.
第二剤
ポリビニルアルコール 12重量%酢酸
ビニルエマルジョン 12重量%カルボキ
シメチルセルロース 10重量%ナイロンパウ
ダー 5重量%防腐剤
適 量プラセンターエキス
適 量精製水
61重量%以上に記載した実施例1.2.3のパ
ック剤について、以下に記載する比較例1,2.3によ
るバック剤と共に、パネル試験により効果を調べた。Second component Polyvinyl alcohol 12% by weight Vinyl acetate emulsion 12% by weight Carboxymethyl cellulose 10% by weight Nylon powder 5% by weight Preservative
Appropriate amount of placenta extract
Appropriate amount of purified water
The effect of the pack agent of Example 1.2.3 described at 61% by weight or more was investigated by a panel test together with the back agent of Comparative Examples 1 and 2.3 described below.
18〜20才未満、20代、30代、40代及び50才
以上の女性パネルそれぞれ5名、20名、20名、20
名、10名の計75名にパック剤を使用してもらい、評
価として、しっとり感、のび、透明感について官能試験
を行った。その結果は第1表の通りである。Female panels aged 18 to under 20, 20s, 30s, 40s, and 50 and over 5, 20, 20, and 20 respectively
A total of 75 people (10 people) used the pack, and a sensory test was conducted to evaluate the moist feel, spreadability, and transparency. The results are shown in Table 1.
(比較例1) 実施例1のポリオキシエチレンオクチル
ドデシルエーテルの代りにデカグリセリンモノステアレ
ートに置き換え、パック剤を調製した。(Comparative Example 1) A pack agent was prepared by replacing polyoxyethylene octyl dodecyl ether in Example 1 with decaglycerin monostearate.
(比較例2) 実施例2のポリオキシエチレンオクチル
ドデシルエーテルの代りにデカグリセリンモノミリステ
ートに置き換えてパック剤を調製した。(Comparative Example 2) A pack agent was prepared by replacing polyoxyethylene octyl dodecyl ether in Example 2 with decaglycerin monomyristate.
(比較例3) 実施例3のポリオキシエチレンオクチル
ドデシルエーテルの代りにデカグリセリンモノステアレ
ートに置き換えてパック剤を調製した。(Comparative Example 3) A pack agent was prepared by replacing the polyoxyethylene octyl dodecyl ether of Example 3 with decaglycerin monostearate.
上記結果から、しっとり感はやや改善され、のびと透明
感は大幅に改善されていることがわかる。From the above results, it can be seen that the moist feeling is slightly improved, and the spreadability and transparency are significantly improved.
さらにのびの評価を摩擦感テスター(カトーテック社K
ES−SE)を用いて測定した。Furthermore, the elongation can be evaluated using a friction tester (Kato Tech Co., Ltd.)
ES-SE).
測定条件
1.被塗布物一多孔質PVA厚さ1關
2.塗布量−0.5ml
3.塗布面積−3X5cm
4.摩擦子−1 0 X 1 0 m+iに0.5m+
Iφピアノ線20本を移動方向に垂直に並べたちの5.
加重−25g
6.移動速度−1關/see
7.測定方法一移動開始5秒後より20秒間測定した。Measurement conditions 1. Object to be coated: Porous PVA thickness: 1:2. Application amount - 0.5ml 3. Application area-3X5cm 4. Friction element-1 0 X 1 0 m+i 0.5m+
5. Arrange 20 Iφ piano wires perpendicular to the moving direction.
Weight -25g 6. Movement speed - 1/see 7. Measurement method: Measurement was carried out for 20 seconds starting 5 seconds after the start of movement.
8.測定感度−2 0 g / v
なお、バラツキはIHz以上の変動を除いた後、実測値
と平均値との差を積分したものを時間で割った値である
。8. Measurement sensitivity -20 g/v Note that the variation is the value obtained by dividing the integrated difference between the actual measurement value and the average value by time after removing fluctuations of IHz or higher.
測定結果を第2表に示す。The measurement results are shown in Table 2.
ただし測定は第1剤のゲルのみを用いた。However, only the gel of the first agent was used for the measurement.
本発明のバック剤の方が、比較例にくらべて、摩擦係数
が小さい。すなわちのびが良好であることを客観的に裏
付けるものである。The backing agent of the present invention has a smaller coefficient of friction than the comparative example. In other words, it objectively proves that the product spreads well.
本発明においては、本出願人による特開昭63−575
08号公報の皮膜形成型化粧用バック剤の2剤型バック
で達或したと同様にしっとり感がよく、剥離時の痛みが
なく、乾燥時の判定が容易で、油剤の浮上等の分離現象
がない等の優れた特性を保持しながら、更にこれに加え
て化粧品として重要なのびや透明感を大幅に改善し、し
っとり感を更に増したパック剤を得ることができた。In the present invention, Japanese Patent Application Laid-open No. 63-575 by the present applicant
Similar to the two-component bag of the film-forming cosmetic backing agent of Publication No. 08, it has a good moist feeling, there is no pain when peeling off, it is easy to determine when it is dry, and there are no separation phenomena such as floating of oil. It was possible to obtain a pack agent that maintains excellent properties such as no dryness, while also significantly improving the spreadability and transparency, which are important for cosmetics, and further increasing the moisturizing feel.
Claims (1)
オキシエチレンオクチルドデシルエーテルを含有する第
一剤と、皮膜形成剤を含有する第二剤とから成る皮膜形
成型化粧用パック剤。A film-forming cosmetic pack comprising a first part containing polyoxyethylene octyl dodecyl ether having a polymerized mole number of ethylene oxide of 10 to 100, and a second part containing a film-forming agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22933289A JPH0818966B2 (en) | 1989-09-06 | 1989-09-06 | Film-forming cosmetic pack |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22933289A JPH0818966B2 (en) | 1989-09-06 | 1989-09-06 | Film-forming cosmetic pack |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0393709A true JPH0393709A (en) | 1991-04-18 |
JPH0818966B2 JPH0818966B2 (en) | 1996-02-28 |
Family
ID=16890496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22933289A Expired - Fee Related JPH0818966B2 (en) | 1989-09-06 | 1989-09-06 | Film-forming cosmetic pack |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0818966B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999022695A1 (en) * | 1997-10-31 | 1999-05-14 | Shiseido Company, Ltd. | Emulsified cosmetic face pack |
-
1989
- 1989-09-06 JP JP22933289A patent/JPH0818966B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999022695A1 (en) * | 1997-10-31 | 1999-05-14 | Shiseido Company, Ltd. | Emulsified cosmetic face pack |
Also Published As
Publication number | Publication date |
---|---|
JPH0818966B2 (en) | 1996-02-28 |
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