JP2004300119A - Oral cavity composition - Google Patents
Oral cavity composition Download PDFInfo
- Publication number
- JP2004300119A JP2004300119A JP2003098410A JP2003098410A JP2004300119A JP 2004300119 A JP2004300119 A JP 2004300119A JP 2003098410 A JP2003098410 A JP 2003098410A JP 2003098410 A JP2003098410 A JP 2003098410A JP 2004300119 A JP2004300119 A JP 2004300119A
- Authority
- JP
- Japan
- Prior art keywords
- gum
- gel
- gelling agent
- oral cavity
- oral
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 210000000214 mouth Anatomy 0.000 title abstract description 24
- 239000000499 gel Substances 0.000 claims abstract description 62
- 239000003349 gelling agent Substances 0.000 claims abstract description 25
- 238000004140 cleaning Methods 0.000 claims abstract description 23
- 229920002148 Gellan gum Polymers 0.000 claims abstract description 13
- 235000010492 gellan gum Nutrition 0.000 claims abstract description 13
- 239000000216 gellan gum Substances 0.000 claims abstract description 13
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 235000010418 carrageenan Nutrition 0.000 claims abstract description 10
- 239000000679 carrageenan Substances 0.000 claims abstract description 10
- 229920001525 carrageenan Polymers 0.000 claims abstract description 10
- 229940113118 carrageenan Drugs 0.000 claims abstract description 10
- -1 furcellaran Polymers 0.000 claims abstract description 10
- 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 claims abstract description 10
- 229920000161 Locust bean gum Polymers 0.000 claims abstract description 7
- 235000010420 locust bean gum Nutrition 0.000 claims abstract description 7
- 239000000711 locust bean gum Substances 0.000 claims abstract description 7
- 229920001277 pectin Polymers 0.000 claims abstract description 7
- 235000010987 pectin Nutrition 0.000 claims abstract description 7
- 239000001814 pectin Substances 0.000 claims abstract description 7
- 240000004584 Tamarindus indica Species 0.000 claims abstract description 6
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- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 claims abstract description 5
- 229920002581 Glucomannan Polymers 0.000 claims abstract description 5
- 229920002678 cellulose Polymers 0.000 claims abstract description 5
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- 229940046240 glucomannan Drugs 0.000 claims abstract description 5
- 229920001817 Agar Polymers 0.000 claims abstract description 4
- 239000008272 agar Substances 0.000 claims abstract description 4
- 235000010443 alginic acid Nutrition 0.000 claims abstract description 4
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- 150000004781 alginic acids Chemical class 0.000 claims abstract description 4
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- 244000215068 Acacia senegal Species 0.000 claims description 4
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- 239000000205 acacia gum Substances 0.000 claims description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 4
- 241000607534 Aeromonas Species 0.000 claims description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- 239000001879 Curdlan Substances 0.000 claims description 3
- 229920002558 Curdlan Polymers 0.000 claims description 3
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- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 239000004373 Pullulan Substances 0.000 claims description 3
- 229920001218 Pullulan Polymers 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
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- 235000019316 curdlan Nutrition 0.000 claims description 3
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- 239000000665 guar gum Substances 0.000 claims description 3
- 229960002154 guar gum Drugs 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
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- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 235000019423 pullulan Nutrition 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 235000002639 sodium chloride Nutrition 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 10
- 210000004400 mucous membrane Anatomy 0.000 abstract description 3
- 210000001519 tissue Anatomy 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 description 6
- 239000002324 mouth wash Substances 0.000 description 5
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 4
- 229910001424 calcium ion Inorganic materials 0.000 description 4
- 210000002200 mouth mucosa Anatomy 0.000 description 4
- 229940051866 mouthwash Drugs 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 3
- 239000001527 calcium lactate Substances 0.000 description 3
- 235000011086 calcium lactate Nutrition 0.000 description 3
- 229960002401 calcium lactate Drugs 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 206010006326 Breath odour Diseases 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 210000005178 buccal mucosa Anatomy 0.000 description 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
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- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
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- 150000007524 organic acids Chemical class 0.000 description 2
- 229960000292 pectin Drugs 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
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- 235000010413 sodium alginate Nutrition 0.000 description 2
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- 238000003756 stirring Methods 0.000 description 2
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- FTLYMKDSHNWQKD-UHFFFAOYSA-N (2,4,5-trichlorophenyl)boronic acid Chemical compound OB(O)C1=CC(Cl)=C(Cl)C=C1Cl FTLYMKDSHNWQKD-UHFFFAOYSA-N 0.000 description 1
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Landscapes
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Abstract
Description
【0001】
【発明の属する技術分野】
本発明は、口腔用組成物に関し、詳しくは、口腔内軟組織(口腔粘膜、舌など)および歯間部の清掃効果に優れた口腔用組成物に関する。
【0002】
【従来の技術】
口腔粘膜(例えば頬粘膜)や舌上のプラークは各種の感染症(例えばカンジダ症)や口臭の原因になることが知られている。現在、口腔粘膜プラークを除去する手段としては、歯ブラシ、タンクリーナー及び洗口剤がある。
【0003】
しかしながら、歯ブラシやタンクリーナーでは頬粘膜を傷つけたり、舌苔を取ろうとすると咽頭を刺激してしまい、洗口剤では清掃効果に乏しい問題があった。
【0004】
一方、歯間部の清掃に関し、歯間ブラシ、フロスなどの物理的清掃手段が知られているが、これらは清掃に時間がかかる不具合があった。
【0005】
歯間部などの清浄化のために、ゲルを用いる口腔内清浄用組成物が知られている(特許文献1(特開2002−193776)及び特許文献2(特開2002−255769))。
【0006】
しかしながら、特許文献1及び特許文献2は、ゲル強度などのゲルの物理化学的性質に問題があり、清浄化効果が不十分であった。
【0007】
本発明は、口腔内、特に口腔粘膜、舌などの口腔内軟組織、歯間部の清浄化効果に優れた口腔用組成物を提供することを目的とする。
【0008】
【特許文献1】
特開2002−193776
【0009】
【特許文献2】
特開2002−255769
【0010】
【課題を解決するための手段】
本発明者は、口腔内軟組織及び歯間部の清掃には、ゲル強度と粘弾性(歪み率)、特にそのバランス、並びに、ゲル化剤の選択/組み合わせが重要であることを見出した。
【0011】
本発明は、以下の口腔用組成物に関する。
項1. 崩壊性ゲルを含む口腔内軟組織または歯間部を清浄化する口腔用組成物。
項2. 崩壊性ゲルが、寒天、カラギーナン、ファーセレラン、アルギン酸及びその塩、ジェランガム及びペクチンからなる群から選ばれる少なくとも1種の第1ゲル化剤とグルコマンナン、ネイティブジェランガム、タラガム、ローカストビーンガム、タマリンド、セルロース類、キサンタンガム、プルラン、グアーガム、カルボキシメチルセルロース塩、デンプンリン酸塩、ポリアクリル酸塩、アラビアガム、カードラン、ガティガム、及びアエロモナスガムからなる群から選ばれる少なくとも1種の第2ゲル化剤とを組み合わせて配合したものである項1に記載の組成物。
【0012】
【発明の実施の形態】
以下、本発明につき更に詳しく説明する。
【0013】
本発明の組成物は、口腔内の清浄化、特に口腔内軟組織及び/又は歯間部の清浄化に適したものである。
【0014】
口腔内軟組織としては、口蓋、頬粘膜、舌、歯茎などが例示される。
【0015】
口腔内軟組織の清浄化は、崩壊性ゲルが軟組織に接触し、軟組織表面の汚れをぬぐい取るように除去する必要があり崩壊性ゲルのゲル強度及び歪み率(粘弾性)が重要になる。ゲル強度と歪み率が適切であれば、適度な強さで軟組織と接触し、ゲルは歪みながら軟組織上の汚れをぬぐい取ることが可能になる。ゲル強度が大きすぎると軟組織との接触時に変形せず、壊れていくため、汚れのぬぐい取り効果が不十分となる。また、ゲル強度が小さすぎると、口中でべたつく感じになり、汚れの除去が困難になる。歪み率(粘弾性)は小さすぎても大きすぎても、汚れを拭い取る力が不十分になる。
【0016】
同様に、歯間部を清浄化する場合、崩壊性ゲルが柔らかすぎたり脆すぎたりすると、十分に歯間部を清掃することができない。一方、崩壊性ゲルの歪み率(粘弾性)が強すぎると、歯間部を清浄化することが困難になる。歯間部を清浄化するためには、崩壊性ゲルのゲル強度、歪み率(粘弾性)のバランスが非常に重要である。ゲル強度を高める場合、第1ゲル化剤が適しているが、歪み率(粘弾性)が不足する傾向にある。一方、歪み率(粘弾性)を高める場合には第2ゲル化剤が適しているが、ゲル強度は不足する傾向にある。
【0017】
従って、歯間部、口腔内軟組織のいずれを清浄化する場合であっても、第1ゲル化剤と第2ゲル化剤を併用し、ゲル強度と歪み率(粘弾性)を所定の範囲内になるように崩壊性ゲルを調製するのが好ましい。
【0018】
本発明の口腔用組成物において、好ましいゲル強度は、10〜300g、より好ましくは30〜250g、さらに好ましくは30〜200gである。
【0019】
好ましい歪み率は、10〜70%、より好ましくは15〜60%、さらに好ましくは15〜50%である。
【0020】
本発明の崩壊性ゲルの好ましいゲル指数は0.1〜10、より好ましくは0.3〜8、さらに好ましくは0.5〜6である。
【0021】
なお、ゲル強度、歪み率、ゲル指数は、以下のようにして測定できる。
<ゲル強度>
測定装置:株式会社サン科学社製 総合物性測定装置(SUN RHCO METRE CR−2000)
測定条件:感圧軸 圧縮弾性用No.1;接触面積 φ10mm;形状 円形
試料台移動速度 10mm/min
測定温度 25℃
<歪み率>
上記機器を用いてゲル強度を測定した際、感圧軸がゲル内へ侵入した距離を測定した。
【0022】
歪み率(%)=100×(ゲル内の侵入距離(mm))/ゲルの高さ(mm)
<ゲル指数>
ゲル指数は、下記式に基づき算出する:
ゲル指数=ゲル内の侵入距離(mm)/歪み率(%)
本発明の崩壊性ゲルを製造するための好ましいゲル化剤の組み合わせとしては、寒天、カラギーナン、ファーセレラン、アルギン酸及びその塩、ジェランガム及びペクチンからなる群から選ばれる少なくとも1種の第1ゲル化剤とグルコマンナン、ネイティブジェランガム、タラガム、ローカストビーンガム、タマリンド、セルロース類、キサンタンガム、プルラン、グアーガム、カルボキシメチルセルロース塩、デンプンリン酸塩、ポリアクリル酸塩、アラビアガム、カードラン、ガティガム及びアエロモナスガムからなる群から選ばれる少なくとも1種の第2ゲル化剤との組み合わせが例示できる。
【0023】
ゲル化剤の全使用量は、通常0.05〜3.0重量%、好ましくは0.1〜1.7重量%である。
【0024】
第1ゲル化剤と第2ゲル化剤を組み合わせて使用する場合、第1ゲル化剤の量は、0.01〜1.0重量%、好ましくは0.05〜0.5重量%、より好ましくは0.05〜0.2重量%であり、第2ゲル化剤の量は、0.01〜2.0重量%、好ましくは0.1〜1.5重量%である。
【0025】
第1ゲル化剤:第2ゲル化剤=1:10〜10:1(重量比)、好ましくは1:5〜5:1(重量比)である。
【0026】
特に好ましいゲル化剤の組み合わせは、
カラギーナン/キサンタンガム/ローカストビーンガム;
ジェランガム/キサンタンガム/ローカストビーンガム;
カラギーナン/グルコマンナン;
ジェランガム/タマリンド;
カラギーナン/タマリンド/ヒドロキシエチルセルロースである。
【0027】
本発明の組成物に使用する崩壊性ゲルは、ゲル化剤を水に加温して溶解させ、冷却して製造することができる。該ゲル化剤溶液にカルシウムイオン、マグネシウムイオン、アルミニウムイオンなどの多価陽イオン、好ましくはアルカリ土類金属イオンを加えることによりゲル化させることも可能である。
【0028】
陽イオン源としては、特に限定されるものではないが、例えば、乳酸カルシウム、乳酸マグネシウム、グルコン酸カルシウム、グリセロリン酸カルシウム、塩化マグネシウム、塩化カルシウム、硫酸マグネシウムなどの有機酸又は無機酸の水溶性多価金属塩が挙げられ、中でも有機酸の塩が好ましく、特に乳酸カルシウムが好ましい。
【0029】
上記したジェランガム、ペクチン、アルギン酸ナトリウム及びカラギーナンの少なくとも1種と多価陽イオンの組み合わせについては、例えば、ジェランガムとカルシウムイオン、ペクチンとカルシウムイオン、カラギーナンとカルシウムイオンが好ましく挙げられる。
【0030】
陽イオン源としての水溶性多価金属塩の配合量は、ジェランガム、ペクチン、アルギン酸ナトリウム及びカラギーナンの少なくとも1種の種類や使用量、所望のゲルの硬さに応じて適宜設定することができるが、通常、組成物全量に基づいて0.01〜2重量%程度、特に0.05〜1重量%程度が好ましい。例えば乳酸カルシウムを陽イオン源として用いる場合には、組成物全重量に基づいて、乳酸カルシウム0.01〜1重量%程度とすればよく、好ましくは0.05〜0.5重量%程度である。他の陽イオン源を用いる場合の使用量は、上記の範囲を参照して適宜設定することができる。
【0031】
本発明組成物のゲルの調製時に用いる水の量は、所期の効果が得られる範囲であれば特に限定されず適宜設定することができるが、ゲルの全重量に基づいて、通常30〜99.9重量%程度、好ましくは50〜99.5重量%程度、より好ましくは70〜99.5%程度である。
【0032】
本発明における口腔内洗浄用組成物のpHとしては、5.0〜7.5程度が好ましく、さらに好ましくは5.5〜7程度である。pHを調整するために緩衝剤を用いることもできる。
【0033】
本発明のゲルには、通常の口腔内洗浄用組成物に使用可能な成分を配合することができる。
【0034】
具体的には、湿潤剤としてエタノール、グリセリン、ソルビット、エチレングリコール、プロピレングリコール、1,3−ブチレングリコール、ポリエチレングリコール、ポリプロピレングリコール、キシリトール、マルチトール、ラクチトール、エリスリトール、パラチノース、パラチニット等が挙げられる。
【0035】
分散剤として、カルボキシメチルセルロースナトリウム,メチルセルロース,ヒドロキシエチルセルロースなどのセルロース誘導体;トラガントガム、カラヤガム、アラビアガム、キサンタンガム、ローカストビーンガムなどのガム類;ポリアクリル酸ナトリウム、ポリオキシエチレンポリオキシプロピレン共重合体、ポリビニルアルコール、カルボキシビニルポリマー、ポリビニルピロリドン等の合成水溶性高分子(通常配合量0.005〜1重量%程度)などが挙げられる。
【0036】
界面活性剤として、ラウリル硫酸ナトリウム、ミリスチル硫酸ナトリウム、N−ラウロイルザルコシネート、ラウロイルメチルタウリン、アシルアミノ酸塩等のアニオン性界面活性剤;ショ糖脂肪酸エステル、ラウリン酸デカグリセリル、ミリスチン酸ジエタノールアミド、ポリオキシエチレン硬化ヒマシ油等の非イオン界面活性剤等(通常配合量0.05〜10重量%)が挙げられる。
【0037】
有効成分として、フッ化ナトリウム、モノフルオロリン酸ナトリウム、フッ化第一錫等のフッ素化合物;デキストラナーゼ、ムタナーゼ、プロテアーゼ、リゾチーム等の酵素;トラネキサム酸、ε−アミノカプロン酸、アルミニウムクロルヒドロキシアラントイン、アラントイン、ジヒドロコレステロール、グリチルリチン酸類、ビサボロール、イソプロピルメチルフェノール、グリセロリン酸、クロロフィル、グルコン酸銅、塩化ナトリウム、水溶性無機リン酸化合物、クロルヘキシジン塩類、トリクロサン、塩化セチルピリジニウム、塩化ベンザルコニウム、塩化ベンゼトニウム;酢酸−dl−α−トコフェロール、酢酸ピリドキシン、アスコルビン酸またはその塩などのビタミン類;タイム、オウゴン等の植物抽出物等が挙げられる。
【0038】
香味剤として、サッカリンナトリウム、アセスルファームカリウム、ステビオサイド、グリチルリチンおよびその塩類、アスパラチルフェニルアラニンメチルエステル、メントール、アネトール、カルボン、オイゲノール、リモネン、ペパーミントオイル、スペアミントオイル、ウインターグリーン、サリチル酸メチル、シオネール、チモール、丁字油、ユーカリ油、ローズマリー油、セージ油、レモン油、オレンジ油、オシメン油、シトロネロール、メチルオイゲノール等通常使用される香味剤であれば特に限定されず配合することができる。
【0039】
着色剤は、公知の色素及び顔料を単独、又は2種以上組み合わせて配合することができる。
【0040】
更に、清掃助剤として、沈降性シリカ、ジルコノシリケート、アルミノシリケート、リン酸カルシウム、炭酸カルシウム、水酸化アルミニウム、酸化アルミニウム等を配合することもできる(配合量10重量%以下)。
【0041】
なお、これら任意成分の配合量は、本発明の効果を妨げない程度で、通常口腔内を洗浄することを目的とする組成物に配合されている程度の量とすればよい。
【0042】
本発明口腔用組成物は、上記のようにして得られた崩壊性ゲルをそのまま用いてもよいし、例えばゲル化後、攪拌や、メッシュを通過させることにより適当な大きさに切断された、ゲルとしてもよい。
【0043】
また、ゲルをポンプ容器から吐出させたり、狭い口を有する軟容器から圧搾して出すことにより、流動性のあるゲルにすることもできる。本発明の組成物は、このようにして使用することができ、また、このようにして得られた流動性のあるゲルも本発明の口腔内洗浄用組成物に含まれる。
【0044】
本発明の口腔内洗浄用組成物は、上記したように、通常の洗口剤のように、口腔内でクチュクチュして、物理的に口腔内軟組織及び歯間部に付着した汚れを拭い取ることにより清浄化するものであり、使用後、口腔中から吐き出すものである。
【0045】
【発明の効果】
本発明の口腔用組成物は、ゲルを口腔内の軟組織と接触させ、或いは歯間部を通過させることにより、ゲルを崩しながらこれらの部位/組織を清浄化するものであり、軟組織に付着したぬめりやプラークを効果的に除去することができ、また、歯間部清掃効果により、口臭、う蝕、歯肉炎、歯周炎などを予防することが可能である。
【0046】
【実施例】
以下、実施例及び比較例を示して本発明を具体的に説明するが、本発明は下記実施例に制限されるものではない。なお、各例中の%はいずれも重量%である。
実施例1〜6及び比較例1〜2
下記表1に示す各成分を用い、崩壊性ゲルから構成される本発明の口腔用組成物を得た。
【0047】
該口腔用組成物について、ゲル強度(g)、歪み率(%)、ゲル指数、洗口のしやすさ、口腔粘膜の清掃感、総合評価について、評価した。これらの結果を併せて表1に示す。
<試料の調製>
ゲル化剤に加水し、分散攪拌しながら約80℃に加温し溶解させた。これにその他の成分を入れ、均一になるまで攪拌した後、冷却固化させて、崩壊性ゲルを得た。
<ゲル強度><歪み率><ゲル指数>
上記方法で調製した試料を前出の方法で測定した。
<官能評価>
10名の専門パネルによる官能評価を行った。
【0048】
上記方法で調製したゲル製剤を平均粒径10mmになるように砕いた。約10mlを口に含み、口内のすみずみまで広げ、頬粘膜や舌などに当たり、歯間部を通過させるようにしながら洗口して、使用感及び清掃感について下記の基準に従い評価した。
*洗口のしやすさ
5;しやすい、4;違和感はない、3;わからない、2;やや違和感あり、1;しにく い
*清掃感
5;かなりあり、4;ややあり、3;わからない、2;あまりない、1;全くない
【0049】
【表1】
[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to an oral composition, and more particularly, to an oral composition having an excellent effect of cleaning oral soft tissues (oral mucosa, tongue, etc.) and interdental regions.
[0002]
[Prior art]
Plaques on the oral mucosa (eg, buccal mucosa) and on the tongue are known to cause various infections (eg, candidiasis) and bad breath. Currently, means for removing oral mucosal plaque include toothbrushes, tank cleaners and mouth washes.
[0003]
However, when using a toothbrush or tank cleaner, the buccal mucous membrane is damaged, or when trying to remove the tongue coating, the pharynx is stimulated, and a mouthwash has a poor cleaning effect.
[0004]
On the other hand, physical cleaning means such as an interdental brush and floss have been known for cleaning the interdental portion, but these have had a problem that it takes a long time to clean.
[0005]
An oral cavity cleaning composition using a gel for cleaning the interdental region and the like is known (Patent Document 1 (JP-A-2002-193776) and Patent Document 2 (JP-A-2002-255768)).
[0006]
However, Patent Literature 1 and Patent Literature 2 have problems in the physicochemical properties of the gel such as gel strength, and the cleaning effect is insufficient.
[0007]
An object of the present invention is to provide a composition for the oral cavity which is excellent in the effect of cleaning the oral cavity, particularly the oral soft tissue such as the oral mucosa and the tongue, and the interdental region.
[0008]
[Patent Document 1]
JP-A-2002-193776
[0009]
[Patent Document 2]
JP-A-2002-255768
[0010]
[Means for Solving the Problems]
The present inventors have found that gel strength and viscoelasticity (strain rate), particularly the balance thereof, and the selection / combination of a gelling agent are important for cleaning oral soft tissues and interdental regions.
[0011]
The present invention relates to the following oral compositions.
Item 1. An oral composition containing a disintegrating gel for cleaning oral soft tissues or interdental regions.
Item 2. Disintegrating gel, agar, carrageenan, furceleran, alginic acid and its salts, at least one first gelling agent selected from the group consisting of gellan gum and pectin and glucomannan, native gellan gum, tara gum, locust bean gum, tamarind, cellulose And at least one second gelling agent selected from the group consisting of xanthan gum, pullulan, guar gum, carboxymethylcellulose salt, starch phosphate, polyacrylate, gum arabic, curdlan, gati gum, and aeromonas gum. Item 2. The composition according to Item 1, which is compounded in combination.
[0012]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, the present invention will be described in more detail.
[0013]
The composition of the present invention is suitable for cleaning the oral cavity, particularly for cleaning oral soft tissues and / or interdental regions.
[0014]
Examples of the soft tissue in the oral cavity include the palate, buccal mucosa, tongue, and gums.
[0015]
In the cleaning of the soft tissue in the oral cavity, it is necessary to remove the disintegrable gel so as to come into contact with the soft tissue and wipe off dirt on the soft tissue surface, and the gel strength and the strain rate (viscoelasticity) of the disintegratable gel become important. If the gel strength and the strain rate are appropriate, the gel will come into contact with soft tissue with an appropriate strength, and the gel will be able to wipe off stains on the soft tissue while being distorted. If the gel strength is too high, the gel does not deform when contacting with soft tissue, but breaks, so that the effect of removing dirt becomes insufficient. On the other hand, if the gel strength is too low, it becomes sticky in the mouth, making it difficult to remove dirt. If the strain rate (viscoelasticity) is too small or too large, the power to wipe off dirt becomes insufficient.
[0016]
Similarly, when cleaning the interdental area, if the disintegrating gel is too soft or too brittle, the interdental area cannot be sufficiently cleaned. On the other hand, if the strain rate (viscoelasticity) of the collapsible gel is too strong, it becomes difficult to clean the interdental region. In order to clean the interdental region, the balance between the gel strength and the strain rate (viscoelasticity) of the collapsible gel is very important. When increasing the gel strength, the first gelling agent is suitable, but the strain rate (viscoelasticity) tends to be insufficient. On the other hand, the second gelling agent is suitable for increasing the strain rate (viscoelasticity), but the gel strength tends to be insufficient.
[0017]
Therefore, regardless of whether the interdental region or the oral soft tissue is to be cleaned, the gel strength and the strain rate (viscoelasticity) are within a predetermined range by using the first gelling agent and the second gelling agent together. It is preferable to prepare a disintegrable gel such that
[0018]
In the oral composition of the present invention, the preferred gel strength is 10 to 300 g, more preferably 30 to 250 g, and still more preferably 30 to 200 g.
[0019]
A preferred strain rate is 10 to 70%, more preferably 15 to 60%, and still more preferably 15 to 50%.
[0020]
The preferred gel index of the disintegratable gel of the present invention is 0.1 to 10, more preferably 0.3 to 8, and still more preferably 0.5 to 6.
[0021]
The gel strength, strain rate, and gel index can be measured as follows.
<Gel strength>
Measuring device: San Kagaku Co., Ltd. Total physical property measuring device (SUN RHCO METER CR-2000)
Measurement conditions: Pressure sensitive shaft No. for compression elasticity 1: Contact area φ10mm; Shape Circular sample stage moving speed 10mm / min
Measurement temperature 25 ℃
<Distortion rate>
When the gel strength was measured using the above instrument, the distance that the pressure-sensitive axis penetrated into the gel was measured.
[0022]
Strain rate (%) = 100 × (penetration distance in gel (mm)) / height of gel (mm)
<Gel index>
The gel index is calculated based on the following formula:
Gel index = Penetration distance in gel (mm) / strain rate (%)
Preferred combinations of gelling agents for producing the disintegrating gel of the present invention include agar, carrageenan, furceleran, alginic acid and salts thereof, at least one first gelling agent selected from the group consisting of gellan gum and pectin, Glucomannan, native gellan gum, cod gum, locust bean gum, tamarind, celluloses, xanthan gum, pullulan, guar gum, carboxymethyl cellulose salts, starch phosphate, polyacrylates, gum arabic, curdlan, gati gum and aeromonas gum And a combination with at least one second gelling agent selected from the group consisting of:
[0023]
The total amount of the gelling agent used is usually 0.05 to 3.0% by weight, preferably 0.1 to 1.7% by weight.
[0024]
When the first gelling agent and the second gelling agent are used in combination, the amount of the first gelling agent is 0.01 to 1.0% by weight, preferably 0.05 to 0.5% by weight, Preferably, it is 0.05 to 0.2% by weight, and the amount of the second gelling agent is 0.01 to 2.0% by weight, preferably 0.1 to 1.5% by weight.
[0025]
The first gelling agent: the second gelling agent = 1: 10 to 10: 1 (weight ratio), preferably 1: 5 to 5: 1 (weight ratio).
[0026]
Particularly preferred combinations of gelling agents are
Carrageenan / xanthan gum / locust bean gum;
Gellan gum / xanthan gum / locust bean gum;
Carrageenan / glucomannan;
Gellan gum / tamarind;
Carrageenan / tamarind / hydroxyethylcellulose.
[0027]
The disintegrable gel used in the composition of the present invention can be produced by dissolving the gelling agent in water by heating and cooling. The gelling agent solution can be gelled by adding a polyvalent cation such as a calcium ion, a magnesium ion or an aluminum ion, preferably an alkaline earth metal ion.
[0028]
The cation source is not particularly limited, but includes, for example, water-soluble polyvalent organic or inorganic acids such as calcium lactate, magnesium lactate, calcium gluconate, calcium glycerophosphate, magnesium chloride, calcium chloride, and magnesium sulfate. Metal salts are mentioned, among which salts of organic acids are preferred, and calcium lactate is particularly preferred.
[0029]
The combination of at least one of the above-mentioned gellan gum, pectin, sodium alginate and carrageenan and a polyvalent cation preferably includes, for example, gellan gum and calcium ions, pectin and calcium ions, and carrageenan and calcium ions.
[0030]
The amount of the water-soluble polyvalent metal salt as the cation source can be appropriately set according to the type and amount of at least one of gellan gum, pectin, sodium alginate, and carrageenan, and the desired gel hardness. Usually, it is preferably about 0.01 to 2% by weight, particularly preferably about 0.05 to 1% by weight based on the total amount of the composition. For example, when calcium lactate is used as a cation source, it may be about 0.01 to 1% by weight, preferably about 0.05 to 0.5% by weight, based on the total weight of the composition. . The amount used when another cation source is used can be appropriately set with reference to the above range.
[0031]
The amount of water used when preparing the gel of the composition of the present invention is not particularly limited as long as the desired effect can be obtained, and can be appropriately set, but is usually 30 to 99 based on the total weight of the gel. It is about 9.9% by weight, preferably about 50 to 99.5% by weight, and more preferably about 70 to 99.5%.
[0032]
The pH of the mouthwash composition of the present invention is preferably about 5.0 to 7.5, and more preferably about 5.5 to 7. Buffers can also be used to adjust the pH.
[0033]
The gel of the present invention can be blended with components that can be used in ordinary compositions for cleaning oral cavity.
[0034]
Specifically, examples of the wetting agent include ethanol, glycerin, sorbit, ethylene glycol, propylene glycol, 1,3-butylene glycol, polyethylene glycol, polypropylene glycol, xylitol, maltitol, lactitol, erythritol, palatinose, and palatinit.
[0035]
As dispersants, cellulose derivatives such as sodium carboxymethylcellulose, methylcellulose and hydroxyethylcellulose; gums such as tragacanth gum, karaya gum, gum arabic, xanthan gum, locust bean gum; sodium polyacrylate, polyoxyethylene polyoxypropylene copolymer, polyvinyl Synthetic water-soluble polymers such as alcohols, carboxyvinyl polymers, and polyvinylpyrrolidone (usually in an amount of about 0.005 to 1% by weight), and the like.
[0036]
Examples of the surfactant include anionic surfactants such as sodium lauryl sulfate, sodium myristyl sulfate, N-lauroyl sarcosinate, lauroylmethyltaurine, and acyl amino acid salts; sucrose fatty acid esters, decaglyceryl laurate, diethanolamide myristate, Nonionic surfactants such as polyoxyethylene hydrogenated castor oil and the like (usually blended amount 0.05 to 10% by weight).
[0037]
Fluorine compounds such as sodium fluoride, sodium monofluorophosphate and stannous fluoride as active ingredients; enzymes such as dextranase, mutanase, protease and lysozyme; tranexamic acid, ε-aminocaproic acid, aluminum chlorohydroxyallantoin, Allantoin, dihydrocholesterol, glycyrrhizic acids, bisabolol, isopropylmethylphenol, glycerophosphoric acid, chlorophyll, copper gluconate, sodium chloride, water-soluble inorganic phosphate compound, chlorhexidine salts, triclosan, cetylpyridinium chloride, benzalkonium chloride, benzethonium chloride; Vitamins such as acetic acid-dl-α-tocopherol, pyridoxine acetate, ascorbic acid or a salt thereof; and plant extracts such as thyme and ogre.
[0038]
As a flavoring agent, saccharin sodium, acesulfame potassium, stevioside, glycyrrhizin and its salts, asparatyl phenylalanine methyl ester, menthol, anethole, carvone, eugenol, limonene, peppermint oil, spearmint oil, wintergreen, methyl salicylate, zionyl, thymol, Any flavoring agent such as clove oil, eucalyptus oil, rosemary oil, sage oil, lemon oil, orange oil, ocimene oil, citronellol, and methyl eugenol can be used without any particular limitation.
[0039]
As the colorant, known dyes and pigments can be used alone or in combination of two or more.
[0040]
Further, as a cleaning aid, sedimentable silica, zirconosilicate, aluminosilicate, calcium phosphate, calcium carbonate, aluminum hydroxide, aluminum oxide and the like can be blended (blending amount: 10% by weight or less).
[0041]
The amount of these optional components may be such that the effects of the present invention are not impaired, and may be such that they are usually incorporated into a composition intended to clean the oral cavity.
[0042]
The oral composition of the present invention may use the disintegrating gel obtained as described above as it is, for example, after gelation, stirring, or cut into an appropriate size by passing through a mesh, It may be a gel.
[0043]
In addition, a gel having fluidity can be obtained by discharging the gel from a pump container or by squeezing the gel out from a soft container having a narrow mouth. The composition of the present invention can be used in this way, and the fluid gel thus obtained is also included in the mouthwash composition of the present invention.
[0044]
As described above, the oral cavity cleaning composition of the present invention is to be punctured in the oral cavity, like a normal mouthwash, to wipe off dirt physically attached to the oral soft tissue and the interdental region. And is exhaled from the oral cavity after use.
[0045]
【The invention's effect】
The oral composition of the present invention cleans these parts / tissues while collapsing the gel by contacting the gel with the soft tissue in the oral cavity or by passing the gel through the interdental region, and adhered to the soft tissue. Slime and plaque can be effectively removed, and the interdental cleaning effect can prevent bad breath, caries, gingivitis, periodontitis, and the like.
[0046]
【Example】
Hereinafter, the present invention will be described specifically with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples. In addition,% in each example is all weight%.
Examples 1-6 and Comparative Examples 1-2
Using the components shown in Table 1 below, an oral composition of the present invention composed of a disintegrable gel was obtained.
[0047]
The composition for oral cavity was evaluated for gel strength (g), strain rate (%), gel index, ease of mouth washing, cleaning feeling of oral mucosa, and comprehensive evaluation. Table 1 also shows these results.
<Preparation of sample>
Water was added to the gelling agent, and the mixture was heated to about 80 ° C. while dispersing and stirring to dissolve. The other components were added thereto, and the mixture was stirred until it became uniform, and then cooled and solidified to obtain a collapsible gel.
<Gel strength><Strainrate><Gelindex>
The sample prepared by the above method was measured by the method described above.
<Sensory evaluation>
Sensory evaluation was performed by a specialized panel of 10 people.
[0048]
The gel preparation prepared by the above method was crushed to have an average particle size of 10 mm. About 10 ml was contained in the mouth, spread to all corners of the mouth, hit the buccal mucous membrane, the tongue, etc., washed the mouth while passing through the interdental region, and evaluated the feeling of use and the feeling of cleaning according to the following criteria.
* Easy to clean mouth 5; Easy 4; No discomfort 3; I do not understand 2; Somewhat uncomfortable 1; Difficult * Cleaning sensation 5; 2, not so much 1; not at all
[Table 1]
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
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| JP2003098410A JP4143829B2 (en) | 2003-04-01 | 2003-04-01 | Oral composition |
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| Application Number | Priority Date | Filing Date | Title |
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| JP2003098410A JP4143829B2 (en) | 2003-04-01 | 2003-04-01 | Oral composition |
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| JP2004300119A true JP2004300119A (en) | 2004-10-28 |
| JP4143829B2 JP4143829B2 (en) | 2008-09-03 |
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| JP2003098410A Expired - Lifetime JP4143829B2 (en) | 2003-04-01 | 2003-04-01 | Oral composition |
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| JP (1) | JP4143829B2 (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006124362A (en) * | 2004-10-27 | 2006-05-18 | Sunstar Inc | Intraoral state-improving composition |
| WO2008001800A1 (en) * | 2006-06-28 | 2008-01-03 | Otsuka Pharmaceutical Co., Ltd. | Tooth enamel dissolution inhibitor |
| KR100814250B1 (en) | 2006-11-01 | 2008-03-17 | 주식회사 엘지생활건강 | Simultaneous Dissolution and Gelled Tablet Oral Hygiene Composition |
| JP2008540631A (en) * | 2005-05-19 | 2008-11-20 | マクニール−ピーピーシー・インコーポレイテッド | Oral care composition with improved directness |
| JP2011032235A (en) * | 2009-08-04 | 2011-02-17 | Sunstar Inc | Liquid oral composition |
| WO2012087324A1 (en) | 2010-12-23 | 2012-06-28 | Colgate-Palmolive Company | Fluid oral care compositions |
| JP2013193969A (en) * | 2012-03-16 | 2013-09-30 | Nippon Zettoc Co Ltd | Gel composition for oral cavity |
| JP2014047179A (en) * | 2012-08-31 | 2014-03-17 | Dsp Gokyo Food & Chemical Co Ltd | Xyloglucan-containing gel composition |
| EP3448356A1 (en) * | 2016-04-29 | 2019-03-06 | Andalay Technologies Limited | Oral composition |
| JP2020083860A (en) * | 2018-11-30 | 2020-06-04 | ライオン株式会社 | Transparent gel composition for rubbing tongue and cleaning method using the same |
| WO2025090845A1 (en) * | 2023-10-26 | 2025-05-01 | Basf Se | Oral care composition |
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- 2003-04-01 JP JP2003098410A patent/JP4143829B2/en not_active Expired - Lifetime
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006124362A (en) * | 2004-10-27 | 2006-05-18 | Sunstar Inc | Intraoral state-improving composition |
| JP2008540631A (en) * | 2005-05-19 | 2008-11-20 | マクニール−ピーピーシー・インコーポレイテッド | Oral care composition with improved directness |
| WO2008001800A1 (en) * | 2006-06-28 | 2008-01-03 | Otsuka Pharmaceutical Co., Ltd. | Tooth enamel dissolution inhibitor |
| EP2039362A4 (en) * | 2006-06-28 | 2011-06-29 | Otsuka Pharma Co Ltd | Tooth enamel dissolution inhibitor |
| JP5419451B2 (en) * | 2006-06-28 | 2014-02-19 | アース製薬株式会社 | Tooth enamel dissolution inhibitor |
| KR100814250B1 (en) | 2006-11-01 | 2008-03-17 | 주식회사 엘지생활건강 | Simultaneous Dissolution and Gelled Tablet Oral Hygiene Composition |
| JP2011032235A (en) * | 2009-08-04 | 2011-02-17 | Sunstar Inc | Liquid oral composition |
| JP2014501256A (en) * | 2010-12-23 | 2014-01-20 | コルゲート・パーモリブ・カンパニー | Oral care fluid composition |
| WO2012087324A1 (en) | 2010-12-23 | 2012-06-28 | Colgate-Palmolive Company | Fluid oral care compositions |
| JP2013193969A (en) * | 2012-03-16 | 2013-09-30 | Nippon Zettoc Co Ltd | Gel composition for oral cavity |
| JP2014047179A (en) * | 2012-08-31 | 2014-03-17 | Dsp Gokyo Food & Chemical Co Ltd | Xyloglucan-containing gel composition |
| EP3448356A1 (en) * | 2016-04-29 | 2019-03-06 | Andalay Technologies Limited | Oral composition |
| US11219580B2 (en) | 2016-04-29 | 2022-01-11 | Andalay Technologies Limited | Oral composition |
| JP2020083860A (en) * | 2018-11-30 | 2020-06-04 | ライオン株式会社 | Transparent gel composition for rubbing tongue and cleaning method using the same |
| JP7138029B2 (en) | 2018-11-30 | 2022-09-15 | ライオン株式会社 | Tongue cleaning transparent gel composition and tongue cleaning method using the same |
| WO2025090845A1 (en) * | 2023-10-26 | 2025-05-01 | Basf Se | Oral care composition |
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