JP6185278B2 - 外用組成物 - Google Patents
外用組成物 Download PDFInfo
- Publication number
- JP6185278B2 JP6185278B2 JP2013095418A JP2013095418A JP6185278B2 JP 6185278 B2 JP6185278 B2 JP 6185278B2 JP 2013095418 A JP2013095418 A JP 2013095418A JP 2013095418 A JP2013095418 A JP 2013095418A JP 6185278 B2 JP6185278 B2 JP 6185278B2
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- Prior art keywords
- composition
- oil
- external
- acid
- gelling agent
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 185
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Description
しかしながら、防腐剤の中には刺激性の観点から、当該組成物への配合量が制限される場合があり、当該組成物に対し、十分な防腐効果や製剤安定性を担保しつつ、良好な使用感を付与することが困難との問題があった。
このような課題を解決するために、油性ゲル化剤を配合した外用組成物にブロック型アルキレンオキシド誘導体を加えることでゲル性能を改善する技術(特許文献4)が報告されている。しかしながら、油性ゲル化剤を配合した外用組成物に、ブチルカルバミン酸ヨウ化プロピニルを添加することは記載されておらず、また使用感、製剤安定性などで十分満足が得られない場合があり、依然改良の余地があった。
(A)ブチルカルバミン酸ヨウ化プロピニル、
(B)油性ゲル化剤
(C)油剤
を含有する外用組成物に関する。
(A)ブチルカルバミン酸ヨウ化プロピニル、
(B)油性ゲル化剤
(C)油剤
を含有することで、外用組成物の真菌に対する防腐効果を増強させる方法に関する。
(A)ブチルカルバミン酸ヨウ化プロピニル、
(B)油性ゲル化剤
(C)油剤
を含有することで、外用組成物の硬度を増加させる方法に関する。
例えば市販品としては、商品名「GLYCASIL(グライカシル)」、「GLYCASIL(グライカシル)2000」、「GLYCASIL(グライカシル)L」「GLYCASIL(グライカシル)S」(いずれも、Lonza社製)等が挙げられる。
例えば、市販品としては、商品名「GP−1(成分名;N−ラウロイル−L−グルタミン酸ジブチルアミド)」(味の素社製)、商品名「EB−1(成分名;N−2−エチルヘキサノイル−L−グルタミン酸ジブチルアミド)」(味の素社製)、商品名「レオパールKL2(表示名称:パルミチン酸デキストリン)」(千葉製粉社製)、商品名「レオパールTL2(表示名称:パルミチン酸デキストリン)」(千葉製粉社製)、商品名「レオパールMKL2(表示名称:ミリスチン酸デキストリン)」(千葉製粉社製)、商品名「レオパールTT2(表示名称:パルミチン酸デキストリン/オクタン酸デキストリン)」(千葉製粉社製)、商品名「レオパールISK2(表示名称:ステアリン酸イヌリン)」(千葉製粉社製)、商品名「ハイマレートPAM(成分名;ポリアミド樹脂)」(高級アルコール工業社製)、商品名「シルバクリアA200V成分名;ポリアミド樹脂)」(アリゾナ ケミカル社製)、商品名「シルバクリアA2614V成分名;ポリアミド樹脂)」(アリゾナ ケミカル社製)、商品名「バーサミド930成分名;ポリアミド樹脂)」(コグニス社製)等が挙げられる。好ましくは、GP−1、レオパールKL2、レオパールMKL2であり、さらに好ましくは、GP−1である。
また成分(A)の含有量は、0.1重量%以下が好ましく、より好ましくは0.05重量%以下、更に好ましくは0.03重量%以下である。0.1重量%以下であれば、十分な防腐効果を有し、刺激性の低い外用組成物を得ることができる。
また成分(B)の含有量は、20重量%以下が好ましく、より好ましくは15重量%以下、更に好ましくは10重量%以下である。20重量%以下であれば、使用感又は、製剤安定性のよい外用組成物が得られる。
成分(B)がN−ラウロイル−L−グルタミン酸ジブチルアミドの場合の含有量は、外用組成物の全量に対して、0.1重量%以上が好ましく、より好ましくは0.5重量%以上、更に好ましくは1重量%以上である。0.1重量%以上であれば、十分な硬度を得ることができる。
また成分(B)の含有量は、10重量%以下が好ましく、より好ましくは7.5重量%以下、更に好ましくは5重量%以下である。10重量%以下であれば、使用感又は、製剤安定性のよい外用組成物が得られる。
成分(B)がN−ラウロイル−L−グルタミン酸ジブチルアミドの場合の含有量は、外用組成物の全量に対して好ましくは0.1重量%以上10重量%以下であり、より好ましくは0.5重量%以上7.5重量%以下であり、更に好ましくは1重量%以上5重量%以下である。
また成分(C)の含有量は、99重量%以下が好ましく、より好ましくは90重量%以下、更に好ましくは80重量%以下である。99重量%以下であれば、良好な使用感の外用組成物が得られる。
また、成分(A)及び成分(B)の含有量の比(A)/(B)は、好ましくは2以下、より好ましくは0.2以下、さらにより好ましくは0.02以下である。2以下であれば、刺激性が少なく、製剤安定性又は使用感のよい外用組成物が得られる。
また本発明にかかる外用組成物を例えば口唇用組成物として使用する場合は、唇に直接組成物を押し付けて塗布し、塗面を清浄にすることなく、そのまま収納する場合が多いため、食物カス、唾液又は皮膚片などが組成物に付着したまま保管され、さらに雑菌が繁殖しやすい環境にあることから、使用時において十分な防腐効果を担保できる本発明にかかる組成物が好適に使用できる。
また、一方で口唇用組成物は大量の油剤を含む場合であっても、油性ゲル化剤を配合することで、組成物に適度な粘性を付与したり、固形状にすることで口唇に塗布しやすく、組成物の滞留性向上等の効果や、相分離を抑制して製剤安定性を改善する効果等を付与できる。
さらに、口唇は人体の中でも非常に敏感な部位で、塗布した組成物が口腔内に入ってしまうことがあるため、使用感や味の点で各成分の配合が制限される場合がある。このため、成分(A)ブチルカルバミン酸ヨウ化プロピニル及び成分(B)油性ゲル化剤を配合することにより、防腐効果及び硬度が相乗的に増加するので、これらの配合量を抑えることができる観点からも、本発明にかかる外用組成物は大変有用である。
等が挙げられる。
また、本発明の外用組成物の室温での硬度は、テクスチャーアナライザーを用いて測定した場合においては、好ましくは2000g以下、より好ましくは1000g以下、さらにより好ましくは800g以下である。2000g以下であれば、使用感のよい製剤が得られる。
ブチルカルバミン酸ヨウ化プロピニルは、細菌類又は真菌類などによる外用組成物の汚染に対する防腐効果を発揮するので、本発明の防腐効果増強方法により防腐効果が増強された外用組成物は、細菌類又は真菌類、好ましくは真菌類、特に好ましくはカンジダ菌(Candida albicans)による汚染を有効に抑えることができる。
硬度増強方法に使用する各成分の種類、外用組成物の使用方法及びその硬度等は、本発明の外用組成物について説明したとおりである。
表1〜3、表5、表7〜9、及び表11に示した各成分を所定量(重量%)で混合し、次いで、加熱撹拌しながら溶解して均一の混合物を得た。該混合物を約25℃に冷却して実施例及び比較例の組成物を得た。
表1に記載の成分を用いて、前記方法に従い、組成物を調製した。
これらの組成物について、第十六改正日本薬局方参考情報 保存効力試験方法に従って、防腐作用を評価した。具体的には、外用組成物の汚染菌として一般的である、真菌のカンジダ菌:Candida albicans(ATCC 10231)を用い、菌液を調製した。菌液を、104〜105CFU/mLになるよう組成物に接種し、25℃で保管した。接種24時間後の組成物をサンプリングし、平板寒天塗抹法にて組成物中の菌数を測定することで生存菌数を求め、比較例1-1の生存菌数を100とし、それぞれの組成物中の生存菌数を比率で示した。
このことから、油剤に、ブチルカルバミン酸ヨウ化プロピニルと油性ゲル化剤を組み合わせることで、高い防腐効果を示すことが確認された。
表2に記載の成分を用いて、前記方法に従い、組成物を調製した。
これらの組成物について、第十六改正日本薬局方参考情報 保存効力試験方法に従って、防腐作用を評価した。具体的には、真菌のカンジダ菌:Candida albicans(ATCC 10231)を用い、それぞれの菌液を調製した。菌液を、104〜105CFU/mLになるよう組成物に接種し、25℃で保管した。接種24時間後の組成物をサンプリングし、平板寒天塗抹法にて組成物中の菌数を測定することで生存菌数を求め、比較例2-1の生存菌数を100として、それぞれの組成物中の生存菌数を比率で示した。
このことから、油剤に、ブチルカルバミン酸ヨウ化プロピニルと低濃度の油性ゲル化剤を組み合わせた場合でも、高い防腐効果を示すことが確認された。
表3に記載の成分を用いて、前記方法に従い組成物を調製し、高温で組成物に流動性がある状態で、各処方10gを直径6cmのガラスシャーレに流し込み、常温で放冷し、固めたものを測定サンプルとした。
テクスチャーアナライザー(製品名:TA.XT.plus Texture Analyser(Stable Micro Systems社製))を用いて、組成物の硬度を測定した。なお、本測定における使用プローブはΦ10mmシリンダープローブであり、具体的な測定条件については、以下表4に示すとおりである。
N−ラウロイル-L-グルタミン酸ジブチルアミドの配合量が0.25、5%の何れの場合においても、ブチルカルバミン酸ヨウ化プロピニルが配合されていない場合(比較例3-1、比較例3-2)と比較して、ブチルカルバミン酸ヨウ化プロピニルを配合した場合(実施例3-1、実施例3-2)には、硬度が相乗的に上昇することが確認された。
表5に記載の成分を用いて、試験例3と同様に、測定サンプルを調製し、テクスチャーアナライザーで、Φ10mmシリンダープローブを用いて硬度を測定した。具体的な測定条件については、以下表6に示すとおりである。
よって、油剤に、油性ゲル化剤とブチルカルバミン酸ヨウ化プロピニルを組み合わせることによって組成物の硬度が上昇するため、油性ゲル化剤の配合量を減らしても所望の硬度を得ることが可能であることが確認された。このことから、スティック状に成型した場合においても、使用感や成形性を考慮して、所望の硬度を有する組成物を得ることが可能であると言える。
表7に記載の成分を用いて、前記方法に従い、組成物を調製した。
これらの組成物について、第十六改正日本薬局方参考情報 保存効力試験方法に従って、防腐作用を評価した。具体的には、真菌のカンジダ菌:Candida albicans(ATCC 10231)を用い、それぞれの菌液を調製した。菌液を、104〜105CFU/mL>になるよう組成物に接種し、25℃で保管した。接種16時間後の組成物をサンプリングし、平板寒天塗抹法にて組成物中の菌数を測定することで生存菌数を求め、比較例4-1の生存菌数を100として、それぞれの組成物中の生存菌数を比率で示した。
このことから、油剤に、高濃度のブチルカルバミン酸ヨウ化プロピニルと油性ゲル化剤を組み合わせた場合でも、相乗的に高い防腐効果を示すことが確認された。
表8に記載の成分を用いて、前記方法に従い、組成物を調製した。
これらの組成物について、第十六改正日本薬局方参考情報 保存効力試験方法に従って、防腐作用を評価した。具体的には、真菌のカンジダ菌:Candida albicans(ATCC 10231)を用い、それぞれの菌液を調製した。菌液を、104〜105CFU/mLになるよう組成物に接種し、25℃で保管した。接種16時間後の組成物をサンプリングし、平板寒天塗抹法にて組成物中の菌数を測定することで生存菌数を求め、比較例5-1の生存菌数を100として、それぞれの組成物中の生存菌数を比率で示した。
このことから、油剤に、低濃度のブチルカルバミン酸ヨウ化プロピニルと油性ゲル化剤を組み合わせた場合でも、相乗的に高い防腐効果を示すことが確認された。
表9に記載の成分を用いて、前記方法に従い組成物を調製し、高温で組成物に流動性がある状態で、各処方10gを直径6cmのガラスシャーレに流し込み、常温で放冷し、固めたものを測定サンプルとした。
テクスチャーアナライザー(製品名:TA.XT.plus Texture Analyser(Stable Micro Systems社製))を用いて、組成物の硬度を測定した。なお、本測定における使用プローブはΦ10mmシリンダープローブであり、具体的な測定条件については、以下表10に示すとおりである。
N−ラウロイル-L-グルタミン酸ジブチルアミドの配合量が1、2.5、5%の何れの場合においても、ブチルカルバミン酸ヨウ化プロピニルが配合されていない場合(比較例6-1、比較例6-2、比較例6-3)と比較して、ブチルカルバミン酸ヨウ化プロピニルを配合した場合(実施例6-1、実施例6-2、実施例6-3)には、硬度が相乗的に上昇することが確認された。
表11に記載の成分を用いて、試験例7と同様に、測定サンプルを調製し、テクスチャーアナライザーで、Φ10mmシリンダープローブを用いて硬度を測定した。具体的な測定条件については、以下表12に示すとおりである。
よって、油剤に、油性ゲル化剤とブチルカルバミン酸ヨウ化プロピニルを組み合わせることによって組成物の硬度が上昇するため、油性ゲル化剤の配合量を減らしても所望の硬度を得ることが可能であることが確認された。このことから、スティック状に成型した場合においても、使用感や成形性を考慮して、所望の硬度を有する組成物を得ることが可能であると言える。
(成分) (重量%)
1.オクチルドデカノール 30
2.流動パラフィン 20
3.リンゴ酸ジイソステアリル 20
4.N−ラウロイル−L−グルタミン酸ジブチルアミド 10
(GP−1)
5.ブチルカルバミン酸ヨウ化プロピニル(IPBC) 0.01
6.ダイマージリノール酸ダイマージリノレイル 19.99
合計 100
(成分) (重量%)
1.イソステアリルアルコール 20
2.水添ポリイソブテン 20
3.ホホバ油 20
4.N-2-エチルヘキサノイル-L-グルタミン酸ジブチルアミド 5
(EB−1)
5.ブチルカルバミン酸ヨウ化プロピニル(IPBC) 0.01
6.2−エチルヘキサン酸セチル 24.99
合計 100
(成分) (重量%)
1.トリイソステアリン酸ポリグリセリル−2 20
2.乳酸オクチルドデシル 10
3.ワセリン 15
4.ミリスチン酸デキストリン(レオパールMKL2) 10
5.ブチルカルバミン酸ヨウ化プロピニル(IPBC) 0.01
6.2−エチルヘキサン酸セチル 44.99
合計 100
(成分) (重量%)
1.イソステアリルアルコール 20
2.乳酸オクチルドデシル 10
3.ワセリン 15
4.ミリスチン酸デキストリン(レオパールMKL2) 1.5
5.N−ラウロイル−L−グルタミン酸ジブチルアミド 3
(GP−1)
6.ブチルカルバミン酸ヨウ化プロピニル(IPBC) 0.01
7.2−エチルヘキサン酸セチル 50.49
合計 100
Claims (10)
- (A)ブチルカルバミン酸ヨウ化プロピニル、(B)油性ゲル化剤及び(C)油剤を含有することを特徴とする外用組成物(但し、エマルジョンの形態であるものを除く)。
- (B)油性ゲル化剤として、アミノ酸系油性ゲル化剤及び脂肪酸デキストリンから選ばれる1種類又は2種類以上を含有することを特徴とする請求項1に記載の外用組成物。
- 前記アミノ酸系油性ゲル化剤として、ラウロイルグルタミン酸ステアリルアミド、N−ラウロイル−L−グルタミン酸ジブチルアミド、又はN−2−エチルヘキサノイル−L−グルタミン酸ジブチルアミドのいずれか1種以上を含むことを特徴とする請求項2に記載の外用組成物。
- 前記脂肪酸デキストリンとして、パルミチン酸デキストリン、ミリスチン酸デキストリン、又はオクタン酸デキストリンのいずれか1種以上を含むことを特徴とする請求項2に記載の外用組成物。
- (C)油剤が、炭化水素油、エステル油、高級アルコール及び天然油から選ばれる1種又は2種以上であることを特徴とする、請求項1〜4のいずれかに記載の外用組成物。
- 口唇用であることを特徴とする、請求項1〜5のいずれかに記載の外用組成物。
- スティック状であることを特徴とする、請求項1〜6のいずれかに記載の外用組成物。
- 室温における硬度が、テクスチャーアナライザーによる測定値で、100g以上2,000g以下である、請求項1〜7のいずれかに記載の外用組成物。
- 外用組成物に(A)ブチルカルバミン酸ヨウ化プロピニル、(B)油性ゲル化剤及び(C)油剤を含有させることを特徴とする、外用組成物における真菌に対する防腐効果の増強方法(但し、上記外用組成物は、エマルジョンの形態であるものを含まない)。
- 外用組成物に(A)ブチルカルバミン酸ヨウ化プロピニル、(B)油性ゲル化剤及び(C)油剤を含有させることを特徴とする、外用組成物における硬度の増加方法(但し、上記外用組成物は、エマルジョンの形態であるものを含まない)。
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