JP2005179290A - 歯磨剤組成物及びその製造方法 - Google Patents
歯磨剤組成物及びその製造方法 Download PDFInfo
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- JP2005179290A JP2005179290A JP2003424331A JP2003424331A JP2005179290A JP 2005179290 A JP2005179290 A JP 2005179290A JP 2003424331 A JP2003424331 A JP 2003424331A JP 2003424331 A JP2003424331 A JP 2003424331A JP 2005179290 A JP2005179290 A JP 2005179290A
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- fatty acid
- triglyceride
- dentifrice
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Abstract
【効果】 本発明は、デキストラナーゼ等のグルカナーゼとノニオン界面活性剤と香料を含有する歯磨剤組成物において、香料による口腔内の刺激を抑え、かつ香り立ちを良好にすると共に、酵素の安定性を確保できるもので、各種剤型に調製して幅広く使用することができる。
【選択図】 なし
Description
[1](a)グルカナーゼ、(b)脂肪酸炭素数が7〜11の脂肪酸のトリグリセライド、(c)アルキル基の炭素数が14〜18で、エチレンオキサイドの平均付加モル数が3〜8のポリオキシエチレンアルキルエーテルとエチレンオキサイドの平均付加モル数が10〜30のポリオキシエチレン硬化ヒマシ油からなるノニオン界面活性剤、(d)香料を0.5〜0.9質量%含有し、成分(b)/成分(d)が質量比で0.10〜0.48でありかつ成分(b)がカプセルに包埋されていないことを特徴とする歯磨剤組成物、及び
[2][1]記載の歯磨剤組成物を製造する方法であって、(c)成分のアルキル基の炭素数が14〜18で、エチレンオキサイドの平均付加モル数が3〜8のポリオキシエチレンアルキルエーテルとエチレンオキサイドの平均付加モル数が10〜30のポリオキシエチレン硬化ヒマシ油とを予め混合してノニオン界面活性剤混合物を調製すると共に、(b)成分の脂肪酸炭素数が7〜11の脂肪酸のトリグリセライドと(d)成分の香料とを予め混合溶解したトリグリセライド・香料混合物を調製し、これらノニオン界面活性剤混合物とトリグリセライド・香料混合物を他成分と混合することを特徴とする[1]記載の歯磨剤組成物の製造方法
を提供する。
R−O−(EO)nH (1)
(Rは炭素数が14〜18のアルキル基、nは3〜8、EOは酸化エチレンを表す。)
で示されるものが使用される。
R1O−CH2−CH(OR2)−CH2−OR3 (2)
(R1、R2、R3は、R4CO−で表される。また、R4は炭素数が6〜10のアルキル基である。)
で示されるものが使用される。
これらの研磨剤の配合量は、歯磨剤組成物全体の2〜40質量%、特に10〜30質量%とすることが好ましい。
これらの配合量は、歯磨剤組成物全体の5〜50質量%、特に20〜45質量%とすることが好ましい。
これらの配合量は、本発明の効果を妨げない範囲で通常量配合することができる。
なお、上記有効成分は、本発明の効果を妨げない範囲で有効量配合することができる。
<1>精製水中に粘結剤、プロピレングリコール、ノニオン界面活性剤、酵素を除く水溶
性成分を常温で混合溶解させたA相を調製する。
<2>プロピレングリコール中に粘結剤を常温で分散させたB相を調製する。
<3>撹拌中のA相の中にB相を添加混合し、更にノニオン界面活性剤混合物を60℃で
添加混合し、C相を調製する。
<4>C相中に、脂肪酸のトリグリセライドと香料(又は脂肪酸のトリグリセライドと香
料との混合物)、酵素、研磨剤等の水溶性成分以外の成分を1.5Lニーダー(石
山商店製)を用いて常温で混合し、減圧による脱泡を行い、歯磨剤組成物を得た。
デキストラナーゼ活性は、歯磨1.0gを採取し、10mMリン酸緩衝液(pH7)25mlを加えて混合分散し、遠心上清1mlを酵素反応液とし、2%デキストラン溶液2mlを酵素基質とし、40℃で20分間反応を行い、分解した還元糖量をソモギーネルソン法にて測定し、以下の基準で評価した。
(酵素安定性の評価基準)
◎:酵素の残存活性(対製造直後の酵素活性)90%以上
○:酵素の残存活性(対製造直後の酵素活性)80%以上90%未満
△:酵素の残存活性(対製造直後の酵素活性)60%以上80%未満
×:酵素の残存活性(対製造直後の酵素活性)60%未満
なお、対照サンプルとして比較例1のサンプルを使用し、これを基準とし評価を行った。
香り立ち
(評点)
3点:対照サンプルと比較して香り立ちが良好
2点:対照サンプルと比較して香り立ちがやや良好
1点:対照サンプルと比較して香り立ちが同等、又は対照サンプルと比較して香り立
ちが悪い
(香り立ち評価基準)
◎:香り立ち平均点 2.0点以上
○:香り立ち平均点 1.5点以上2.0点未満
×:香り立ち平均点 1.5点未満
口腔内の刺激の程度
(評点)
3点:対照サンプルと比較して刺激が弱い
2点:対照サンプルと比較して刺激がやや弱い
1点:対照サンプルと比較して刺激が同等、又は対照サンプルと比較して刺激が強い
(口腔内の刺激評価基準)
◎:口腔内の刺激平均点 2.0点以上
○:口腔内の刺激平均点 1.5点以上2.0点未満
×:口腔内の刺激平均点 1.5点未満
以下に結果を示す。なお、表1〜4中の配合量を表す数値はいずれも質量%である。
*カプセル化
カプセル内容液として、香料組成物([表4]の香料J)75質量%、成分(b)25質量%、被膜形成物質として、寒天50質量%、グリセリン45質量%、精製水5質量%を用い、滴下法(特開平8−325127号公報記載の寒天粒子製造例1の方法参照)によりカプセル(親油成分包埋寒天粒子)を製造した。
このカプセル(被膜率[カプセル全質量中の被膜形成物質の質量%]20質量%、平均粒子径1000μm)を、歯磨組成中に1.0質量%配合した。
Claims (2)
- (a)グルカナーゼ、(b)脂肪酸炭素数が7〜11の脂肪酸のトリグリセライド、(c)アルキル基の炭素数が14〜18で、エチレンオキサイドの平均付加モル数が3〜8のポリオキシエチレンアルキルエーテルとエチレンオキサイドの平均付加モル数が10〜30のポリオキシエチレン硬化ヒマシ油からなるノニオン界面活性剤、(d)香料を0.5〜0.9質量%含有し、成分(b)/成分(d)が質量比で0.10〜0.48でありかつ成分(b)がカプセルに包埋されていないことを特徴とする歯磨剤組成物。
- 請求項1記載の歯磨剤組成物を製造する方法であって、(c)成分のアルキル基の炭素数が14〜18で、エチレンオキサイドの平均付加モル数が3〜8のポリオキシエチレンアルキルエーテルとエチレンオキサイドの平均付加モル数が10〜30のポリオキシエチレン硬化ヒマシ油とを予め混合してノニオン界面活性剤混合物を調製すると共に、(b)成分の脂肪酸炭素数が7〜11の脂肪酸のトリグリセライドと(d)成分の香料とを予め混合溶解したトリグリセライド・香料混合物を調製し、これらノニオン界面活性剤混合物とトリグリセライド・香料混合物を他成分と混合することを特徴とする請求項1記載の歯磨剤組成物の製造方法。
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2007055976A (ja) * | 2005-08-26 | 2007-03-08 | Lion Corp | 練歯磨組成物 |
JP2008308463A (ja) * | 2007-06-18 | 2008-12-25 | Lion Corp | 歯磨剤組成物 |
WO2009087474A3 (en) * | 2008-01-08 | 2009-09-03 | Akthelia Pharmaceuticals | Agonists for antimicrobial peptide systems |
JP2022519437A (ja) * | 2018-12-19 | 2022-03-24 | エルブイエムエイチ レシェルシェ | 液状化粧料 |
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US20090229178A1 (en) | 2006-07-20 | 2009-09-17 | Weder Donald E | Method of wrapping a floral grouping |
US20080016763A1 (en) | 2006-07-20 | 2008-01-24 | Weder Donald E | Method for wrapping a floral grouping |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007055976A (ja) * | 2005-08-26 | 2007-03-08 | Lion Corp | 練歯磨組成物 |
JP2008308463A (ja) * | 2007-06-18 | 2008-12-25 | Lion Corp | 歯磨剤組成物 |
WO2009087474A3 (en) * | 2008-01-08 | 2009-09-03 | Akthelia Pharmaceuticals | Agonists for antimicrobial peptide systems |
US9078864B2 (en) | 2008-01-08 | 2015-07-14 | Akthelia Pharmaceuticals | Agonists for antimicrobial peptide systems |
JP2022519437A (ja) * | 2018-12-19 | 2022-03-24 | エルブイエムエイチ レシェルシェ | 液状化粧料 |
JP7485270B2 (ja) | 2018-12-19 | 2024-05-16 | エルブイエムエイチ レシェルシェ | 液状化粧料 |
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