JP2005068071A - 口腔用組成物及び口腔用組成物中におけるラウリル硫酸カリウムの析出防止方法 - Google Patents
口腔用組成物及び口腔用組成物中におけるラウリル硫酸カリウムの析出防止方法 Download PDFInfo
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- JP2005068071A JP2005068071A JP2003299544A JP2003299544A JP2005068071A JP 2005068071 A JP2005068071 A JP 2005068071A JP 2003299544 A JP2003299544 A JP 2003299544A JP 2003299544 A JP2003299544 A JP 2003299544A JP 2005068071 A JP2005068071 A JP 2005068071A
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- oral composition
- sodium
- lauryl sulfate
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- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 7
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- 238000000622 liquid--liquid extraction Methods 0.000 description 1
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- 239000004325 lysozyme Substances 0.000 description 1
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- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
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- 229910000400 magnesium phosphate tribasic Inorganic materials 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 235000010981 methylcellulose Nutrition 0.000 description 1
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- 239000010502 orange oil Substances 0.000 description 1
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- 229930007459 p-menth-8-en-3-one Natural products 0.000 description 1
- 108700009886 palmitoyl sarcosine Proteins 0.000 description 1
- AXCXHFKZHDEKTP-UHFFFAOYSA-N para-methoxycinnamaldehyde Natural products COC1=CC=C(C=CC=O)C=C1 AXCXHFKZHDEKTP-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 210000002379 periodontal ligament Anatomy 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229940057838 polyethylene glycol 4000 Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- OQZCJRJRGMMSGK-UHFFFAOYSA-M potassium metaphosphate Chemical compound [K+].[O-]P(=O)=O OQZCJRJRGMMSGK-UHFFFAOYSA-M 0.000 description 1
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- 230000002829 reductive effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010668 rosemary oil Substances 0.000 description 1
- 229940058206 rosemary oil Drugs 0.000 description 1
- 239000010670 sage oil Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
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Abstract
【効果】 硝酸カリウムとラウリル硫酸ナトリウムとの併用配合により低温析出を抑制し得、硝酸カリウムの有効性が十分に発揮されるもので、象牙質知覚過敏症の予防及び治療に有効である。
【選択図】 なし
Description
(i)(a)硝酸カリウム及び(b)ラウリル硫酸ナトリウムを含有する口腔用組成物に、(c)多価アルコールを組成物全体の10質量%以上60質量%以下と、(d)両性界面活性剤とが配合され、前記(b):(d)が質量比で50:1〜1:1の範囲であることを特徴とする口腔用組成物、
(ii)(a)硝酸カリウム及び(b)ラウリル硫酸ナトリウムを含有する口腔用組成物において、硝酸カリウムとラウリル硫酸ナトリウムとの反応により生成するラウリル硫酸カリウムの析出を防止する方法であって、前記口腔用組成物に(c)多価アルコールを組成物全体の10質量%以上60質量%以下を配合すると共に、(d)両性界面活性剤を前記(b)成分:(d)成分が質量比で50:1〜1:1の範囲となるように配合することを特徴とする前記口腔用組成物中におけるラウリル硫酸カリウムの析出防止方法
を提供する。
下記表1に示す組成の歯磨組成物を常法により調製した。なお、表1の組成、更には後述する実施例において使用した香料組成は表2〜7に示す通りである。
得られた歯磨組成物について、下記方法及び基準により低温析出評価及び知覚過敏抑制評価を行ったところ、表1のような結果が得られた。
各種歯磨剤を10℃恒温槽にて4週間保存した後、10gを紙面に出し、下記基準により評価した。
○:表面上にも内部にも析出は全くない。
△:表面上に析出はないが、内部に析出あり。
×:表面上、内部ともに析出あり。
知覚過敏抑制評価:
各練歯磨を象牙質知覚過敏症の症状のある人8名に約4週間使用させ、下記基準により評価した。
○:痛みを感じなくなり、改善した。
△:ある程度改善したが、痛みを感じる。
×:使用前と変わらず痛みを感じ、改善しない。
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.5
グリセリン 30
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 1.0
モノフルオロリン酸ナトリウム 0.73
プロピレングリコール 4.0
カラギーナン 0.8
ヒドロキシエチルセルロース 0.4
サッカリンナトリウム 0.02
無水ケイ酸 14
香料B 0.8
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.5
ソルビトール 24
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 1.0
モノフルオロリン酸ナトリウム 0.73
乳酸アルミニウム 2.0
水酸化ナトリウム 0.5
プロピレングリコール 4.0
カルボキシメチルセルロースナトリウム 0.8
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
無水ケイ酸 14
香料C 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
ソルビトール 24
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 1.0
モノフルオロリン酸ナトリウム 0.73
乳酸アルミニウム 2.0
塩化セチルピリジニウム 0.05
水酸化ナトリウム 0.5
プロピレングリコール 4.0
キサンタンガム 0.5
カルボキシメチルセルロースナトリウム 0.2
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
無水ケイ酸 13
香料D 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
ソルビトール 24
ポリエチレングリコール400 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
フッ化ナトリウム 0.73
乳酸アルミニウム 2.0
塩化セチルピリジニウム 0.05
水酸化ナトリウム 0.5
プロピレングリコール 4.0
キサンタンガム 0.5
カルボキシメチルセルロースナトリウム 0.2
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
無水ケイ酸 18
香料E 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 2.0
ソルビトール 24
プロピレングリコール 4.0
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
モノフルオロリン酸ナトリウム 0.73
トラネキサム酸 0.05
水酸化ナトリウム 0.2
キサンタンガム 0.5
カルボキシメチルセルロースナトリウム 0.2
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
無水ケイ酸 18
香料F 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
ソルビトール 15
ポリエチレングリコール4000 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
モノフルオロリン酸ナトリウム 0.73
乳酸アルミニウム 2.0
トリクロサン 0.05
水酸化ナトリウム 0.2
プロピレングリコール 4.0
ヒドロキシエチルセルロース 1.0
サッカリンナトリウム 0.02
炭酸カルシウム 30
香料G 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
ソルビトール 15
ポリエチレングリコール400 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
モノフルオロリン酸ナトリウム 0.73
乳酸アルミニウム 2.0
イプシロンアミノカプロン酸 0.05
水酸化ナトリウム 0.2
プロピレングリコール 4.0
カラギーナン 0.5
カルボキシメチルセルロースナトリウム 0.2
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
リン酸水素カルシウム 30
香料H 1.0
精製水 残
計 100.0%
以下の処方のジェル組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
グリセリン 30
ポリエチレングリコール400 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
フッ化ナトリウム 0.73
ヒドロキシエチルセルロース 2.0
サッカリンナトリウム 0.02
香料I 1.0
精製水 残
計 100.0%
以下の処方の洗口液を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 0.1
グリセリン 20
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
ポリオキシエチレン硬化ヒマシ油 0.4
サッカリンナトリウム 0.02
香料B 1.0
精製水 残
計 100.0%
以下の処方の歯磨組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
ソルビトール 8.0
マンニトール 5.0
ポリエチレングリコール400 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
モノフルオロリン酸ナトリウム 0.73
プロピレングリコール 4.0
カラギーナン 0.5
カルボキシメチルセルロースナトリウム 0.2
ヒドロキシエチルセルロース 0.3
サッカリンナトリウム 0.02
炭酸水素カルシウム 30
香料C 1.0
精製水 残
計 100.0%
以下の処方のジェル組成物を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 1.0
キシリトール 15
ポリエチレングリコール400 0.4
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
ヒドロキシエチルセルロース 2.0
サッカリンナトリウム 0.02
香料D 1.0
精製水 残
計 100.0%
以下の処方の洗口液を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 0.1
マルチトール 18
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
ポリオキシエチレン硬化ヒマシ油 1.0
サッカリンナトリウム 0.02
香料E 1.0
精製水 残
計 100.0%
以下の処方の洗口液を、常法に従い製造した。
成分名 配合量(%)
硝酸カリウム 5.0
ラウリル硫酸ナトリウム 0.1
パラチノース 14
2−アルキル−N−カルボキシメチル
−N−ヒドロキシエチルイミダゾリニウムベタイン
(エナジコールC−40H) 0.1
ポリオキシエチレン硬化ヒマシ油 1.5
サッカリンナトリウム 0.02
香料F 1.0
精製水 残
計 100.0%
上記実施例7〜19の口腔用組成物は、いずれも低温析出が抑制され、優れた象牙質知覚過敏抑制効果を有していた。
Claims (5)
- (a)硝酸カリウム及び(b)ラウリル硫酸ナトリウムを含有する口腔用組成物に、(c)多価アルコールを組成物全体の10質量%以上60質量%以下と、(d)両性界面活性剤とが配合され、前記(b)成分:(d)成分が質量比で50:1〜1:1の範囲であることを特徴とする口腔用組成物。
- (c)成分の多価アルコールが、グリセリン、ポリエチレングリコ−ル、ソルビトール、プロピレングリコール、マンニトール、キシリトール、マルチトール、パラチノースから選ばれる1種又は2種以上である請求項1記載の口腔用組成物。
- (d)成分の両性界面活性剤が、アルキルイミダゾリニウムベタイン又はその塩から選ばれる1種又は2種以上である請求項1又は2記載の口腔用組成物。
- 象牙質知覚過敏症の予防及び治療用である請求項1〜3のいずれか1項記載の口腔用組成物。
- (a)硝酸カリウム及び(b)ラウリル硫酸ナトリウムを含有する口腔用組成物において、硝酸カリウムとラウリル硫酸ナトリウムとの反応により生成するラウリル硫酸カリウムの析出を防止する方法であって、前記口腔用組成物に(c)多価アルコールを組成物全体の10質量%以上60質量%以下を配合すると共に、(d)両性界面活性剤を前記(b)成分:(d)成分が質量比で50:1〜1:1の範囲となるように配合することを特徴とする前記口腔用組成物中におけるラウリル硫酸カリウムの析出防止方法。
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