JP6715698B2 - 液体口腔用組成物 - Google Patents
液体口腔用組成物 Download PDFInfo
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- JP6715698B2 JP6715698B2 JP2016125156A JP2016125156A JP6715698B2 JP 6715698 B2 JP6715698 B2 JP 6715698B2 JP 2016125156 A JP2016125156 A JP 2016125156A JP 2016125156 A JP2016125156 A JP 2016125156A JP 6715698 B2 JP6715698 B2 JP 6715698B2
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- NWZBFJYXRGSRGD-UHFFFAOYSA-M sodium;octadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCOS([O-])(=O)=O NWZBFJYXRGSRGD-UHFFFAOYSA-M 0.000 description 1
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- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Landscapes
- Cosmetics (AREA)
Description
(A)アシルグルタミン酸、及びアシルメチルタウリンから選ばれるアシルアミノ酸又はその塩 0.01質量%以上0.3質量%以下
(B)香料
(C)両性界面活性剤 0.1質量%以上1.5質量%以下
(D)水 50質量%以上95質量%以下
を含有し、成分(B)の含有量と成分(C)の含有量との質量比((B)/(C))が0.05以上1.5以下であり、かつノニオン界面活性剤の含有量が成分(C)の含有量以下であり、かつ25℃におけるpHが6以上である液体口腔用組成物に関する。
本発明の液体口腔用組成物は、成分(A)として、アシルグルタミン酸、及びアシルメチルタウリンから選ばれるアシルアミノ酸又はその塩を0.01質量%以上0.3質量%以下含有する。かかる成分(A)を特定の量で含有することにより、良好な汚れ除去性能を有しつつ、優れた発泡性を発現することができる。
なお、吸油量とは、シリカが担持できる油量を示したものであり、測定方法はJIS K5101−13−2(2004年制定)に基づく方法により、吸収される煮あまに油の量により特定する。
なお、本発明の液体口腔用組成物の25℃におけるpHを上記範囲に調整する上で、pH調整剤を用いてもよい。かかるpH調整剤としては、炭酸塩や重炭酸塩;水酸化カリウムや水酸化ナトリウム;クエン酸、リンゴ酸、乳酸、酒石酸、コハク酸等の有機酸又はこれらの塩から選ばれる1種又は2種以上が挙げられる。なかでも、炭酸塩、重炭酸塩が好ましく、炭酸ナトリウム、炭酸水素ナトリウム、セスキ炭酸ナトリウムが好ましい。この場合、pH調整剤の含有量は、液体口腔用組成物のpHを安定化させる観点から、本発明の液体口腔用組成物中に、好ましくは0.1〜2質量%であり、より好ましくは0.15〜1.5質量%であり、さらに好ましくは0.18〜1質量%であり、よりさらに好ましくは0.2〜0.8質量%である。
なお、上記ポリエチレングリコールの平均分子量とは、GPC(ゲルパーミェーションクロマトグラフィ)により測定される質量平均分子量を意味する。
表1〜2に示す処方にしたがって、25℃におけるpHを10に調整した液体口腔用組成物を製造し、以下の方法にしたがって、各評価を行った。
結果を表1〜2に示す。
また、本発明の液体口腔用組成物において、成分(B)の香料として用い得る具体的な香料を表4〜6に示す。なお、実施例1〜15、及び比較例1〜4では、表4に示す香料を用いた。
得られた各液体口腔用組成物をガラス瓶に充填し、ガラス瓶の外側から内容物の液体口腔用組成物を目視により観察し、以下の基準にしたがって評価した。
A:透明で均一であった
B:多少白濁していたものの、均一であった
C:白濁していたものの、析出物までは確認されなかった
D:分離又は析出物が確認された
得られた各液体口腔用組成物をガラス瓶に充填し、−5℃で10日間保存した後、ガラス瓶の外側から内容物の液体口腔用組成物を目視により観察し、上記「製造直後の外観」と同様の基準にしたがって評価した。
得られた各液体口腔用組成物をガラス瓶に充填し、−5℃で10日間保存した後、BL粘度計(東機産業(株)社製、M1ローター、回転数:30rpm/1分間)を用い、−5℃に保持したまま液粘度(mPa・s)を測定した。
得られた各液体口腔用組成物100gをポンプフォーマー容器(F5ポンプフォーマー、メッシュ:2枚、メッシュサイズ:#255/#255、大和製罐(株))に充填し、吐出口から内容物を吐出させ、BH粘度計(東機産業(株)社製、H2ローター、回転数:5rpm/1分間)を用い、室温(25℃)にて泡粘度(mPa・s)を測定した。
得られた各液体口腔用組成物100gを上記ポンプフォーマー容器に充填し、室温(25℃)にて、ろ紙(ADVANTEC No.1、70mm)を5枚重ねた上に、吐出口から約1gの内容物を吐出させた。吐出後30秒経過した時点で泡をふき取り、ろ紙の重量変化を測定し(排液量)、以下の計算式から排液率(%)を算出した。排液率の数値が低いほど泡持ちがよいことを意味する。
排液率(%)=(排液量)/(泡吐出重量)×100
表3に示す処方にしたがって、25℃におけるpHを10に調整して製造した液体口腔用組成物は、長期にわたり優れた低温保存安定性を発揮し、かつ透明性が高い。
Claims (6)
- 次の成分(A)、(B)、(C)、並びに(D):
(A)アシルグルタミン酸、及びアシルメチルタウリンから選ばれるアシルアミノ酸又はその塩 0.01質量%以上0.3質量%以下
(B)香料
(C)両性界面活性剤 0.1質量%以上1.5質量%以下
(D)水 50質量%以上95質量%以下
を含有し、成分(B)の含有量と成分(C)の含有量との質量比((B)/(C))が0.05以上1.5以下であり、かつノニオン界面活性剤の含有量が成分(C)の含有量以下であるか、或いはノニオン界面活性剤を含有せず、
かつ25℃におけるpHが6以上である、泡吐出容器に充填されてなる液体口腔用組成物。 - アルキル硫酸塩(E)を含有し、かつ成分(E)の含有量と成分(C)の含有量との質量比((E)/(C))が、1.7以下である請求項1に記載の液体口腔用組成物。
- 成分(E)の含有量と成分(A)の含有量との質量比((E)/(A))が、1以上50以下である請求項2に記載の液体口腔用組成物。
- 成分(E)の含有量が、0.1質量%以上1.5質量%以下である請求項2又は3に記載の液体口腔用組成物。
- 成分(B)の含有量が、0.1質量%以上1.5質量%以下である請求項1〜4のいずれか1項に記載の液体口腔用組成物。
- 透明又は半透明である請求項1〜5のいずれか1項に記載の液体口腔用組成物。
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