JP2012219038A - Composition for oral cavity - Google Patents
Composition for oral cavity Download PDFInfo
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- JP2012219038A JP2012219038A JP2011084218A JP2011084218A JP2012219038A JP 2012219038 A JP2012219038 A JP 2012219038A JP 2011084218 A JP2011084218 A JP 2011084218A JP 2011084218 A JP2011084218 A JP 2011084218A JP 2012219038 A JP2012219038 A JP 2012219038A
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- water
- oral cavity
- fluorine
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- 239000000203 mixture Substances 0.000 title claims abstract description 70
- 210000000214 mouth Anatomy 0.000 title claims abstract description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 51
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims abstract description 35
- 150000002016 disaccharides Chemical class 0.000 claims abstract description 30
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 claims abstract description 19
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims abstract description 19
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims abstract description 19
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 3
- 150000005846 sugar alcohols Chemical class 0.000 claims description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 11
- 239000011230 binding agent Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 abstract description 26
- 239000011737 fluorine Substances 0.000 abstract description 26
- 230000000694 effects Effects 0.000 abstract description 11
- 208000002925 dental caries Diseases 0.000 abstract description 10
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 7
- 210000004268 dentin Anatomy 0.000 abstract description 7
- 230000002265 prevention Effects 0.000 abstract description 4
- -1 fluorine ions Chemical class 0.000 description 26
- 210000003298 dental enamel Anatomy 0.000 description 20
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 9
- PVXPPJIGRGXGCY-DJHAAKORSA-N 6-O-alpha-D-glucopyranosyl-alpha-D-fructofuranose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@](O)(CO)O1 PVXPPJIGRGXGCY-DJHAAKORSA-N 0.000 description 8
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 8
- 239000000551 dentifrice Substances 0.000 description 8
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 8
- 229940091249 fluoride supplement Drugs 0.000 description 7
- 239000000594 mannitol Substances 0.000 description 7
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 6
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 6
- 229910001424 calcium ion Inorganic materials 0.000 description 6
- 235000010355 mannitol Nutrition 0.000 description 6
- 239000004386 Erythritol Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 235000019414 erythritol Nutrition 0.000 description 5
- 229940009714 erythritol Drugs 0.000 description 5
- 239000011775 sodium fluoride Substances 0.000 description 5
- 235000013024 sodium fluoride Nutrition 0.000 description 5
- 239000000600 sorbitol Substances 0.000 description 5
- 229930195725 Mannitol Natural products 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- 235000019640 taste Nutrition 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 3
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 3
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 235000019606 astringent taste Nutrition 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- FBPFZTCFMRRESA-UHFFFAOYSA-N hexane-1,2,3,4,5,6-hexol Chemical compound OCC(O)C(O)C(O)C(O)CO FBPFZTCFMRRESA-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 239000000606 toothpaste Substances 0.000 description 2
- 229940034610 toothpaste Drugs 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 239000000811 xylitol Substances 0.000 description 2
- 235000010447 xylitol Nutrition 0.000 description 2
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 2
- 229960002675 xylitol Drugs 0.000 description 2
- 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 2
- SVBWNHOBPFJIRU-UHFFFAOYSA-N 1-O-alpha-D-Glucopyranosyl-D-fructose Natural products OC1C(O)C(O)C(CO)OC1OCC1(O)C(O)C(O)C(O)CO1 SVBWNHOBPFJIRU-UHFFFAOYSA-N 0.000 description 1
- SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 description 1
- 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 1
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- XGRSAFKZAGGXJV-UHFFFAOYSA-N 3-azaniumyl-3-cyclohexylpropanoate Chemical compound OC(=O)CC(N)C1CCCCC1 XGRSAFKZAGGXJV-UHFFFAOYSA-N 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- GUBGYTABKSRVRQ-CUHNMECISA-N D-Cellobiose 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)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-CUHNMECISA-N 0.000 description 1
- UNXHWFMMPAWVPI-QWWZWVQMSA-N D-Threitol Chemical class OC[C@@H](O)[C@H](O)CO UNXHWFMMPAWVPI-QWWZWVQMSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- 102000051366 Glycosyltransferases Human genes 0.000 description 1
- 108700023372 Glycosyltransferases Proteins 0.000 description 1
- 241000511976 Hoya Species 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- FBPFZTCFMRRESA-BXKVDMCESA-N L-mannitol Chemical compound OC[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)CO FBPFZTCFMRRESA-BXKVDMCESA-N 0.000 description 1
- 229930182842 L-mannitol Natural products 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 108010039918 Polylysine Proteins 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- 241000194019 Streptococcus mutans Species 0.000 description 1
- 206010047642 Vitiligo Diseases 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KXKPYJOVDUMHGS-OSRGNVMNSA-N chondroitin sulfate Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](OS(O)(=O)=O)[C@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(O)=O)O1 KXKPYJOVDUMHGS-OSRGNVMNSA-N 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 210000004513 dentition Anatomy 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- OVYSUCIJMISHSX-UHFFFAOYSA-N hexan-1-amine;hydrofluoride Chemical compound F.CCCCCCN OVYSUCIJMISHSX-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000905 isomalt Substances 0.000 description 1
- 235000010439 isomalt Nutrition 0.000 description 1
- HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229940096017 silver fluoride Drugs 0.000 description 1
- REYHXKZHIMGNSE-UHFFFAOYSA-M silver monofluoride Chemical compound [F-].[Ag+] REYHXKZHIMGNSE-UHFFFAOYSA-M 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229960004711 sodium monofluorophosphate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- YUOWTJMRMWQJDA-UHFFFAOYSA-J tin(iv) fluoride Chemical compound [F-].[F-].[F-].[F-].[Sn+4] YUOWTJMRMWQJDA-UHFFFAOYSA-J 0.000 description 1
- 230000036346 tooth eruption Effects 0.000 description 1
- NMXLJRHBJVMYPD-IPFGBZKGSA-N trehalulose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CO[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 NMXLJRHBJVMYPD-IPFGBZKGSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
本発明は、フッ素イオン供給化合物及び水への溶解度が低い二糖類を含有する口腔用組成物に関する。 The present invention relates to a composition for oral cavity containing a fluoride ion supplying compound and a disaccharide having low solubility in water.
歯質の主成分はハイドロキシアパタイトであり、口中においては通常、リン酸イオンやカルシウムイオンの溶出(脱灰)と、リン酸カルシウムやハイドロキシアパタイトへの結晶化(再石灰化)が平衡状態にある。歯のう蝕は、ストレプトコッカス・ミュータンス(Streptococcus mutans)等の細菌がショ糖等を分解して有機酸を産生しpHを低下させ、歯のカルシウム等を溶出させることにより脱灰を促進することで進行していく。う蝕の初期段階においては、エナメル質に白斑(ホワイトスポット)といわれる歯の表層下脱灰病巣を生じる。ここでフッ素イオンはカルシウムイオンとリン酸イオンの結晶化、すなわち再石灰化を促進することにより、う蝕の発生を防止し、かかる白斑を消失させうることが知られている。 The main component of the tooth is hydroxyapatite, and in the mouth, the elution (decalcification) of phosphate ions and calcium ions and the crystallization (remineralization) to calcium phosphate and hydroxyapatite are usually in an equilibrium state. Dental caries promotes decalcification by causing bacteria such as Streptococcus mutans to decompose sucrose to produce organic acids, lowering the pH, and eluting tooth calcium etc. It will progress in. In the initial stages of caries, enamel produces subsurface demineralized lesions of the teeth called white spots. Here, it is known that fluorine ions can prevent the occurrence of caries and eliminate such vitiligo by promoting crystallization of calcium ions and phosphate ions, that is, remineralization.
一方、トレハロースやトレハルロース等の二糖類は、渋味や収斂感等の雑味を低減して、良好な味や使用感をもたらすことが知られており(例えば、特許文献1)、またう蝕の発生を有効に防止する作用をももたらすことから、これを配合した飲食物や化粧品、医薬品等も報告されている(例えば、特許文献2)。更に、トレハロース等の二糖類によるう蝕予防効果を発揮させる技術として、トレハロースとキシリトールやソルビトール等の糖アルコールとポリリジン又はその塩を含有する口腔用組成物も開示されている(例えば、特許文献3)。このように、トレハロース等の二糖類を含有させると、味の改善を図ることができるだけでなく、う蝕の発生防止にも大いに寄与し得る。 On the other hand, disaccharides such as trehalose and trehalulose are known to reduce miscellaneous taste such as astringency and astringency, and to provide a good taste and feeling of use (for example, Patent Document 1). Since it also has the effect | action which prevents the generation | occurrence | production of this effectively, the food / beverage products and cosmetics, pharmaceuticals, etc. which mix | blended this are also reported (for example, patent document 2). Furthermore, a composition for oral cavity containing trehalose, a sugar alcohol such as xylitol, sorbitol, and polylysine or a salt thereof is also disclosed as a technique for exerting a caries prevention effect by a disaccharide such as trehalose (for example, Patent Document 3). ). Thus, when a disaccharide such as trehalose is contained, not only can the taste be improved, but it can greatly contribute to the prevention of caries.
こうしたなか、更なるう蝕予防・再石灰化促進を図るべく、フッ素イオン供給化合物とトレハロース等の二糖類とを併用した技術として、特許文献4には、トレハロースとフッ素イオン供給物質とカルシウムイオン供給物質を含有する口腔用組成物が開示されており、トレハロースとカルシウムイオンとで複合体が形成されることによって、プラークへのカルシウムイオンの付着量が増大することが示されている。 Under these circumstances, Patent Document 4 discloses trehalose, a fluoride ion supply substance, and calcium ion supply as a technique in which a fluorine ion supply compound and a disaccharide such as trehalose are used in combination to further prevent dental caries and promote remineralization. An oral composition containing a substance has been disclosed, and it is shown that the amount of calcium ions attached to plaques is increased by the formation of a complex between trehalose and calcium ions.
歯のエナメル質又は象牙質にフッ素イオンを取り込ませ、再石灰化を促進するためには、フッ素イオン濃度を高くすることが考えられるが、フッ素イオンの溶解性、安全性の観点から大量に口腔用組成物に含有させることは困難であり、少量のフッ素イオンを効率的にエナメル質又は象牙質に取り込ませることが望ましい。しかしながら、特許文献4に記載の口腔用組成物は、フッ素イオン供給化合物を併用しているものの、もっぱらカルシウムイオンのプラークへの滞留性の向上を図ることを主たる課題としており、フッ素イオンを効率よくエナメル質に取り込ませるための処方については充分な検討がなされていない。そのため、前述の特許文献に開示された口腔用組成物を用いたとしても、歯のエナメル質又は象牙質へのフッ素イオンの取り込み量を充分に確保することはできない。 In order to incorporate fluoride ions into the tooth enamel or dentin and promote remineralization, it may be possible to increase the fluoride ion concentration. It is difficult to contain the composition in the composition, and it is desirable to efficiently incorporate a small amount of fluorine ions into the enamel or dentin. However, although the composition for oral cavity described in Patent Document 4 is used in combination with a fluorine ion supply compound, it is mainly intended to improve the retention of calcium ions in plaque, and fluorine ions are efficiently used. Sufficient studies have not been made on prescriptions for incorporation into enamel. Therefore, even if the composition for oral cavity disclosed in the above-mentioned patent document is used, it is not possible to ensure a sufficient amount of fluorine ions taken into the tooth enamel or dentin.
したがって、本発明の課題は、トレハロース等の二糖類とフッ素イオン供給化合物とを併用しながら、歯のエナメル質又は象牙質へのフッ素イオンの取り込み量を増大させることによって、歯の耐酸性を向上させ、う蝕予防効果を充分に期待できる口腔用組成物を提供することにある。 Therefore, the object of the present invention is to improve the acid resistance of teeth by increasing the amount of fluoride ions taken into tooth enamel or dentin while using a disaccharide such as trehalose in combination with a fluoride ion supplying compound. An object of the present invention is to provide an oral composition capable of sufficiently expecting a caries prevention effect.
そこで本発明者らは、トレハロース等の二糖類に対して水の量が多すぎると、歯のエナメル質等に対するフッ素イオン取り込み量を充分に確保できないおそれがあるとの新たなる知見に基づき、さらに水に対する溶解度の低い二糖類を用いることで、フッ素イオン供給化合物を併用しつつ、水分量を一定の範囲に調整し、二糖類と水分を一定の比率とすることにより、歯のエナメル質又は象牙質に対するフッ素イオンの取り込み量が顕著に増大し、歯の耐酸性を向上させ、う蝕を抑制する効果に優れた口腔用組成物が得られることを見出した。 Therefore, the present inventors based on the new finding that if the amount of water is too large relative to disaccharides such as trehalose, there is a possibility that sufficient fluoride ion uptake amount for tooth enamel etc. may not be secured. By using disaccharides with low solubility in water, the amount of water is adjusted to a certain range while using a fluoride ion supply compound, and the ratio of disaccharides and moisture is made constant, thereby enamel or dental dentition of teeth. It was found that the amount of fluorine ions taken up with respect to the quality significantly increases, the acid resistance of the teeth is improved, and an oral composition excellent in the effect of suppressing caries can be obtained.
すなわち、本発明は、次の成分(A)、(B)及び(C):
(A)20℃における水に対する溶解度が50質量%以下である二糖類 25〜50質量%、
(B)水 10〜40質量%、
(C)フッ素イオン供給化合物 フッ素原子換算で0.002〜5質量%
を含有し、成分(A)と成分(B)の質量比(A/B)が1〜4である口腔用組成物を提供するものである。
That is, the present invention comprises the following components (A), (B) and (C):
(A) 25-50 mass% of disaccharides whose solubility in water at 20 ° C. is 50 mass% or less,
(B) 10 to 40% by mass of water,
(C) Fluorine ion supply compound 0.002 to 5% by mass in terms of fluorine atoms
The composition for oral cavity in which the mass ratio (A / B) of a component (A) and a component (B) is 1-4 is contained.
本発明の口腔用組成物を用いれば、フッ素イオン供給化合物のフッ素イオンが効率よくエナメル質又は象牙質に取り込まれるため、歯の耐酸性を向上させ、う蝕を抑制する効果が向上する。 If the composition for oral cavity of this invention is used, since the fluorine ion of a fluorine ion supply compound will be taken in efficiently in an enamel or dentin, the acid resistance of a tooth will be improved and the effect which suppresses a caries will improve.
以下、本発明について詳細に説明する。
本発明の口腔用組成物は、20℃における水に対する溶解度が50質量%以下である二糖類(A)を含有する。二糖類とは、単糖が2分子結合したものであり、上記溶解度とは、20℃における飽和水溶液100質量%中の二糖類の溶解量(質量%)を意味する。本発明に用いられる、20℃における水に対する溶解度が50質量%以下の二糖類(A)としては、具体的には、例えば、ラクトース(20℃における水への溶解度:21質量%)、トレハロース(20℃における水への溶解度:41質量%)、パラチノース(20℃における水への溶解度:39質量%)、セロビオース(20℃における水への溶解度:14%)等を挙げることができる。これらは1種単独で用いてもよく、2種以上組み合わせて用いてもよい。なかでも、歯のエナメル質等に効率よくフッ素イオンを取り込ませつつ、適度な粘度と物性を得る点で、20℃における水に対する溶解度が20〜45質量%の二糖類が好ましく、具体的にはトレハロース、パラチノースが好ましく、さらにトレハロースが好ましい。
Hereinafter, the present invention will be described in detail.
The composition for oral cavity of this invention contains the disaccharide (A) whose solubility with respect to water in 20 degreeC is 50 mass% or less. The disaccharide is obtained by bonding two molecules of monosaccharides, and the solubility means the dissolved amount (% by mass) of the disaccharide in 100% by mass of a saturated aqueous solution at 20 ° C. Specific examples of the disaccharide (A) having a solubility in water at 20 ° C. of 50% by mass or less used in the present invention include lactose (solubility in water at 20 ° C .: 21% by mass), trehalose ( Examples thereof include solubility in water at 20 ° C .: 41% by mass, palatinose (solubility in water at 20 ° C .: 39% by mass), cellobiose (solubility in water at 20 ° C .: 14%), and the like. These may be used alone or in combination of two or more. Among them, a disaccharide having a solubility in water at 20 ° C. of 20 to 45% by mass is preferable from the viewpoint of obtaining appropriate viscosity and physical properties while efficiently incorporating fluorine ions into tooth enamel and the like. Specifically, Trehalose and palatinose are preferable, and trehalose is more preferable.
上記二糖類(A)は、歯のエナメル質等に対するフッ素イオン取り込み量増大効果の点から、本発明の口腔用組成物中に、25〜50質量%含有し、より好ましくは30〜50質量%、さらに好ましくは30〜45質量%含有する。 The disaccharide (A) is contained in the composition for oral cavity of the present invention in an amount of 25 to 50% by mass, more preferably 30 to 50% by mass, from the viewpoint of the effect of increasing the amount of fluorine ions taken into the tooth enamel and the like. More preferably, it contains 30 to 45% by mass.
本発明の口腔用組成物における水(B)の含有量は、歯のエナメル質等へのフッ素イオン取り込み量増大効果の点から重要であり、10〜40質量%であって、12〜35質量%が好ましく、15〜30質量%がより好ましく、15〜25質量%がさらに好ましい。水(B)を10〜40質量%含有し、成分(A)の二糖類を水(B)以上の質量で含有することによって、未溶解状態の二糖類(A)を存在させつつ、組成物に構造粘性をもたせ、含有される水(B)に溶解したフッ素イオン供給化合物(C)のフッ素イオンの流動性を確保することができると考えられる。また、二糖類(A)の水への溶解量が少ないため、水(B)中のフッ素イオン供給物(C)のフッ素イオン濃度を高くすることができ、高濃度のフッ素イオンが流動して歯に接触すると考えられる。こうして本発明の口腔用組成物は、歯のエナメル質等へのフッ素イオン取り込み量を高くすることができる。なお、水(B)には配合した精製水以外に、例えば配合に用いる糖アルコール(F)の水溶液等に含有される水分も含まれる。 The content of water (B) in the composition for oral cavity of the present invention is important from the viewpoint of the effect of increasing the amount of fluorine ions taken into the enamel of teeth, and is 10 to 40% by mass, and is 12 to 35% by mass. % Is preferable, 15 to 30% by mass is more preferable, and 15 to 25% by mass is further preferable. A composition containing 10 to 40% by mass of water (B) and containing the disaccharide of component (A) in a mass greater than or equal to water (B) while allowing the undissolved disaccharide (A) to exist. It is considered that the fluidity of the fluorine ions of the fluorine ion supply compound (C) dissolved in the water (B) contained therein can be secured by imparting a structural viscosity. In addition, since the amount of disaccharide (A) dissolved in water is small, the fluorine ion concentration of the fluoride ion supply (C) in water (B) can be increased, and the high concentration of fluorine ions flows. It is thought to contact the teeth. Thus, the composition for oral cavity of the present invention can increase the amount of fluorine ions taken into the enamel of teeth. The water (B) includes water contained in, for example, an aqueous solution of a sugar alcohol (F) used for blending in addition to the purified water blended.
また、本発明の口腔用組成物は、高い構造粘性をもつことが好ましく、組成物100質量部に対して、25質量部の水を加えて希釈した場合に、希釈後の粘度は希釈前の粘度に対して15%以下に低下するものが好ましく、より好ましくは10%以下に低下する。 The oral composition of the present invention preferably has a high structural viscosity. When 100 parts by weight of the composition is diluted by adding 25 parts by weight of water, the viscosity after dilution is the same as before dilution. What falls to 15% or less with respect to a viscosity is preferable, More preferably, it falls to 10% or less.
本発明の口腔用組成物は、二糖類(A)と水(B)の質量比(A/B)が1〜4であり、水(B)よりも二糖類(A)の質量が大きいことが好ましく、常温(20℃)において口腔用組成物中に飽和溶解状態を越えて含有され、未溶解状態の二糖類(A)が存在するものが好ましい。未溶解状態の二糖類(A)を存在させることによって組成物に構造粘性を持たせつつ、溶解した二糖類(A)によるフッ素イオンの流動性低下を抑制し、水(B)に溶解されたフッ素イオン供給化合物(C)のフッ素イオンの流動性を確保する観点から、二糖類(A)と水(B)の質量比(A/B)は、1より大きく3以下が好ましく、さらに1より大きく3未満が好ましい。 The composition for oral cavity of the present invention has a mass ratio (A / B) of disaccharide (A) and water (B) of 1 to 4, and the mass of disaccharide (A) is larger than that of water (B). It is preferable that it is contained in the oral composition at a room temperature (20 ° C.) exceeding the saturated dissolution state and the disaccharide (A) in an undissolved state is present. The presence of the undissolved disaccharide (A) allowed the composition to have structural viscosity, while suppressing the decrease in fluidity of fluorine ions due to the dissolved disaccharide (A), and the composition was dissolved in water (B). From the viewpoint of securing the fluidity of the fluoride ions of the fluoride ion supply compound (C), the mass ratio (A / B) of the disaccharide (A) to the water (B) is preferably greater than 1 and less than or equal to 3; Largely less than 3 is preferable.
本発明の口腔用組成物は、フッ素イオン供給化合物(C)を含有する。フッ素イオン供給化合物は、フッ素化合物であって、水溶液においてフッ素イオンを放出する化合物をいう。当該フッ素イオン供給化合物は、無機化合物、有機化合物のいずれであってもよい。具体的には、フッ化ナトリウム、フッ化カリウム、フッ化スズ、フッ化ケイ素酸ナトリウム、フッ化アンモニウム、フッ化アルミニウム、フッ化銀、フッ化水素酸ヘキシルアミン、フッ化水素酸デカノールアミン、フッ化水素酸オクタデセニルアミン等が挙げられ、歯のエナメル質等へのフッ素イオン取り込み量が高い点から、フッ化ナトリウム、フッ化アンモニウムが好ましく、特にフッ化ナトリウムが好ましい。これらのフッ素イオン供給化合物は、1種単独で用いてもよく、2種以上組み合わせて用いてもよい。また、フッ素イオンを直接供給しない、フッ素イオン供給化合物(C)以外のフッ素化合物として、モノフルオロリン酸ナトリウムを併用することもできる。 The composition for oral cavity of the present invention contains a fluorine ion supply compound (C). The fluorine ion supply compound is a fluorine compound that releases fluorine ions in an aqueous solution. The fluorine ion supply compound may be an inorganic compound or an organic compound. Specifically, sodium fluoride, potassium fluoride, tin fluoride, sodium fluoride siliconate, ammonium fluoride, aluminum fluoride, silver fluoride, hexylamine hydrofluoride, decanolamine hydrofluoride, Examples thereof include octadecenylamine hydrofluorate, and sodium fluoride and ammonium fluoride are preferred, and sodium fluoride is particularly preferred from the viewpoint of high fluorine ion uptake into tooth enamel and the like. These fluorine ion supply compounds may be used alone or in combination of two or more. Moreover, sodium monofluorophosphate can also be used together as fluorine compounds other than the fluorine ion supply compound (C) which do not supply a fluorine ion directly.
フッ素イオン供給化合物(C)は、歯のエナメル質等に対するフッ素イオン取り込み量を充分に確保する点及び安全性の点から、本発明の口腔用組成物中、フッ素イオンに換算して0.002〜5質量%含有し、より好ましくは0.01〜1質量%、さらに好ましくは0.05〜0.5質量%含有する。 The fluoride ion supply compound (C) is 0.002 in terms of fluoride ion in the oral composition of the present invention from the viewpoint of ensuring a sufficient amount of fluoride ion uptake with respect to tooth enamel and the like and safety. -5% by mass, more preferably 0.01-1% by mass, and still more preferably 0.05-0.5% by mass.
本発明の口腔用組成物は、さらに20℃における水に対する溶解度の40質量%以下の、溶解度の低い糖アルコール(E)を含有してもよい。本発明に用いることのできる、20℃における水に対する溶解度が40質量%以下の糖アルコール(E)としては、エリスリトール、マンニトール、α−D−グルコピラノシル−1,6−ソルビトール、α−D−グルコピラノシル−1,6−マンニトール、α−D−グルコピラノシル−1,6−ソルビトールとα−D−グルコピラノシル−1,6−マンニトールの混合物である還元パラチノース等が挙げられる。 The composition for oral cavity of the present invention may further contain a sugar alcohol (E) having a low solubility of 40% by mass or less of the solubility in water at 20 ° C. Examples of the sugar alcohol (E) having a solubility in water at 20 ° C. of 40% by mass or less that can be used in the present invention include erythritol, mannitol, α-D-glucopyranosyl-1,6-sorbitol, α-D-glucopyranosyl- Examples include 1,6-mannitol, reduced palatinose, which is a mixture of α-D-glucopyranosyl-1,6-sorbitol and α-D-glucopyranosyl-1,6-mannitol.
本発明で用いるエリスリトールは、L−エリスリトール、D−エリスリトール、meso−エリスリトールの3種の異性体のいずれの構造であってもよいし、混合物であってもよい。結晶状のエリスリトールは、市販品としては、日研化学(株)、三菱化学フーズ(株)、セレスター社製等のものが入手可能である。エリスリトールの20℃における水に対する溶解度は33質量%である。 The erythritol used in the present invention may have a structure of any of the three isomers of L-erythritol, D-erythritol, and meso-erythritol, or may be a mixture. As crystalline erythritol, commercially available products such as those manufactured by Nikken Chemical Co., Ltd., Mitsubishi Chemical Foods Co., Ltd., and Celestor are available. The solubility of erythritol in water at 20 ° C. is 33% by mass.
マンニトールは、ヘキシトールの一種でありマンノースの糖アルコールである。工業的には、トウモロコシデンプン糖の電解還元、蔗糖の高圧還元により生産されている。本発明で用いるマンニトールは、D−マンニトール、L−マンニトール、D,L−マンニトールから選ばれる少なくとも1種であればよく、特に限定されるものではないが、天然界に存在するD−マンニトールが入手容易であり、好ましい。マンニトールの20℃における水への溶解度は、18質量%である。 Mannitol is a kind of hexitol and is a sugar alcohol of mannose. Industrially, it is produced by electrolytic reduction of corn starch sugar and high-pressure reduction of sucrose. The mannitol used in the present invention is not particularly limited as long as it is at least one selected from D-mannitol, L-mannitol, and D, L-mannitol, but D-mannitol existing in nature is available. Easy and preferred. The solubility of mannitol in water at 20 ° C. is 18% by mass.
還元パラチノースは、二糖類の糖アルコールであり、α−D−グルコピラノシル−1,6ーマンニトール及びその異性体であるα−D−グルコピラノシル−1,6ーソルビトールの等モル混合物である。還元パラチノースは、シュクロースを原料とし、シュクロースを糖転移酵素によりパラチノースとした後に、水素添加反応させることによって得られる。また、還元パラチノースは、市販品としては、三井製糖社、及びSudzucker AG社(和名:南独製糖)の商品名「パラチニット」が入手可能であり、イソマルトという別名称もある。還元パラチノースの20℃における水への溶解度は、28質量%である。 Reduced palatinose is a disaccharide sugar alcohol and is an equimolar mixture of α-D-glucopyranosyl-1,6-mannitol and its isomer α-D-glucopyranosyl-1,6-sorbitol. Reduced palatinose is obtained by using sucrose as a raw material, converting sucrose to palatinose with a glycosyltransferase, and then performing a hydrogenation reaction. In addition, as the reduced palatinose, commercially available product names “Palatinite” from Mitsui Sugar Co., Ltd. and Suducker AG (Japanese name: South German Sugar Co., Ltd.) are available, and there is another name called isomalt. The solubility of reduced palatinose in water at 20 ° C. is 28% by mass.
これらの糖アルコール(E)は1種又は2種以上を混合して用いることができる。また、糖アルコール(E)は粉体、粒状のいずれを配合してもよい。 These sugar alcohols (E) can be used alone or in combination of two or more. Moreover, sugar alcohol (E) may mix | blend any of powder and a granular form.
これらの糖アルコール(E)を含有する場合、歯のエナメル質等に対するフッ素イオン取り込み量増大効果の点から、本発明の口腔用組成物中に、0質量%を超え30質量%以下含有するのが好ましく、さらに1〜20質量%が好ましく、さらに5〜15質量%含有するのがより好ましい。また、本発明の水への溶解性の低い二糖類(A)と糖アルコール(E)の合計含有量の水(B)に対する質量比((A+E)/B)は、組成物に構造粘性を持たせつつ、水(B)に溶解されたフッ素イオン供給化合物(C)のフッ素イオンの流動性を確保する観点から、1〜6であることが好ましく、1〜4であることがより好ましく、さらに1より大きく3.5以下であることが好ましい。 When these sugar alcohols (E) are contained, the composition for oral cavity of the present invention contains more than 0% by mass and not more than 30% by mass from the viewpoint of the effect of increasing the amount of fluorine ions taken into the enamel of teeth. Is preferable, 1-20 mass% is more preferable, and it is more preferable to contain 5-15 mass% further. In addition, the mass ratio ((A + E) / B) of the total content of the disaccharide (A) and the sugar alcohol (E) having low solubility in water according to the present invention to the water (B) gives the composition a structural viscosity. From the viewpoint of ensuring the fluidity of the fluorine ions of the fluorine ion supply compound (C) dissolved in water (B) while having it, it is preferably 1 to 6, more preferably 1 to 4, Further, it is preferably larger than 1 and not larger than 3.5.
また、本発明の口腔用組成物は、湿潤効果、使用感の点から、歯のエナメル質等への高いフッ素取り込み量を阻害しない範囲で、さらに、20℃における水に対する溶解度が40質量%を超える他の糖アルコール(F)を含有してもよい。他の糖アルコール(F)としては、具体的には、例えば、キシリトール(20℃における水への溶解度:66質量%)、ソルビトール(20℃における水への溶解度:72質量%)が挙げられる。 Further, the composition for oral cavity of the present invention has a solubility in water at 20 ° C. of 40% by mass as long as it does not hinder high fluorine uptake into tooth enamel and the like from the viewpoint of moistening effect and feeling of use. You may contain the other sugar alcohol (F) exceeding. Specific examples of the other sugar alcohol (F) include xylitol (solubility in water at 20 ° C .: 66% by mass) and sorbitol (solubility in water at 20 ° C .: 72% by mass).
他の糖アルコール(F)を含有する場合には、歯のエナメル質等への高いフッ素取り込み量を確保する点から、本発明の口腔用組成物中の含有量は、20質量%以下が好ましく、15質量%以下がより好ましく、12質量%以下がさらに好ましい。また、水(B)に溶解されたフッ素イオン供給化合物(C)のフッ素イオンの流動性を確保する観点から、他の糖アルコール(F)の口腔用組成物に含有される水(B)に対する質量比(F/B)が1未満であることが好ましく、0.8以下であることがより好ましい。 When other sugar alcohols (F) are contained, the content in the oral composition of the present invention is preferably 20% by mass or less from the viewpoint of securing a high fluorine uptake amount in the tooth enamel and the like. 15 mass% or less is more preferable, and 12 mass% or less is further more preferable. Moreover, from the viewpoint of ensuring the fluidity of the fluorine ions of the fluorine ion supply compound (C) dissolved in water (B), the water (B) contained in the oral composition of other sugar alcohols (F). The mass ratio (F / B) is preferably less than 1, and more preferably 0.8 or less.
本発明の口腔用組成物は、フッ素イオンを歯のエナメル質又は象牙質へ効率よく取り込ませる点から、グリセリンを含有するのが望ましい。グリセリンを含有する場合、良好な味と使用感をも保持する点から、本発明の口腔用組成物中に1〜30質量%含有するのが好ましく、さらに5〜20質量%含有するのが好ましい。 The oral composition of the present invention preferably contains glycerin from the viewpoint of efficiently incorporating fluorine ions into the tooth enamel or dentin. When it contains glycerin, it is preferable to contain 1-30 mass% in the composition for oral cavity of this invention from the point which hold | maintains a favorable taste and usability, Furthermore, it is preferable to contain 5-20 mass%. .
本発明の口腔用組成物は、さらに粘結剤(D)を含有するのが好ましい。粘結剤(D)としては、カルボキシメチルセルロースナトリウム、ヒドロキシエチルセルロース、カルボキシビニルポリマー、キサンタンガム、カラギーナン、アルギン酸ナトリウム、ヒドロキシプロピルセルロース、コンドロイチン硫酸ナトリウム等が挙げられ、カルボキシメチルセルロースナトリウム、キサンタンガム、カラギーナンが好ましい。これらは1種単独で用いてもよく、2種以上組み合わせて用いてもよい。 It is preferable that the composition for oral cavity of the present invention further contains a binder (D). Examples of the binder (D) include sodium carboxymethylcellulose, hydroxyethylcellulose, carboxyvinyl polymer, xanthan gum, carrageenan, sodium alginate, hydroxypropylcellulose, sodium chondroitin sulfate and the like, and sodium carboxymethylcellulose, xanthan gum and carrageenan are preferable. These may be used alone or in combination of two or more.
粘結剤(D)は、ゲル状歯磨組成物のゲル化用、ペースト状歯磨組成物又は練り歯磨組成物の粘結用、又は塗布用組成物の粘結用として配合される。本発明においては、口腔用組成物中の粘結剤(D)の含有量は、水(B)中のフッ素イオンの流動性を確保する観点から、0.1〜1.5質量%が好ましく、さらに1.2質量%以下が好ましく、より好ましくは1.0質量%未満、さらに0.8質量%以下であることが好ましく、口腔用組成物の吐出性や歯ブラシ上での保形性、又は塗布用組成物の歯牙への滞留性の観点から0.1質量%以上であることが好ましく、さらに0.3質量%以上であることが好ましい。 The binder (D) is blended for gelation of a gel-like dentifrice composition, for caking of a paste-like dentifrice composition or a toothpaste composition, or for caking of a coating composition. In the present invention, the content of the binder (D) in the composition for oral cavity is preferably 0.1 to 1.5% by mass from the viewpoint of securing the fluidity of fluorine ions in water (B). Further, 1.2% by mass or less is preferable, more preferably less than 1.0% by mass, and further preferably 0.8% by mass or less, dischargeability of the oral composition and shape retention on the toothbrush, Or it is preferable that it is 0.1 mass% or more from a viewpoint of the staying property to the tooth of the coating composition, and also it is preferable that it is 0.3 mass% or more.
本発明の口腔用組成物には、前記成分の他、本発明の効果を阻害しない範囲で、発泡剤、発泡助剤、研磨剤、成分(D)以外の湿潤剤、甘味剤、保存料、殺菌剤、薬効成分、顔料、色素、香料等を適宜含有させることができる。なお、フッ素イオンと不溶性塩を形成する成分は、歯のエナメル質等へのフッ素イオンの取り込み促進効果を阻害するおそれがある。フッ素イオンと不溶性塩を形成する成分としては、炭酸カルシウム、リン酸カルシム、ヒドロキシアパタイト等のカルシウム塩が挙げられ、本発明の口腔用組成物中のこれらの含有量は2質量%以下が好ましく、1質量%以下がより好ましく、0.1質量%以下がさらに好ましい。また、フッ素イオンと不溶性塩を形成する成分として、クエン酸等の3塩基酸やエチレンジアミン四酢酸等の酸も挙げられ、本発明の口腔用組成物中のこれらの酸の含有量は、0.1質量%未満が好ましく、0.05質量%未満がより好ましく、0.01質量%以下がさらに好ましい。また、本発明の口腔用組成物は、例えば、ゲル状、ペースト状といった剤形に調製され、練り歯磨組成物、ゲル状歯磨組成物等の歯磨組成物、塗布用口腔用組成物等にすることができる。 In the composition for oral cavity of the present invention, in addition to the above-mentioned components, a foaming agent, a foaming aid, an abrasive, a wetting agent other than component (D), a sweetening agent, a preservative, Bactericides, medicinal components, pigments, dyes, fragrances and the like can be appropriately contained. In addition, the component which forms an insoluble salt with fluoride ion may inhibit the effect of promoting the incorporation of fluoride ion into tooth enamel and the like. Examples of the component that forms an insoluble salt with fluoride ions include calcium salts such as calcium carbonate, calcium phosphate, hydroxyapatite, and the content of these in the oral composition of the present invention is preferably 2% by mass or less. 1 mass% or less is more preferable, and 0.1 mass% or less is further more preferable. In addition, examples of components that form insoluble salts with fluoride ions include tribasic acids such as citric acid and acids such as ethylenediaminetetraacetic acid. The content of these acids in the oral composition of the present invention is 0.00. The amount is preferably less than 1% by mass, more preferably less than 0.05% by mass, and still more preferably 0.01% by mass or less. The oral composition of the present invention is prepared in a dosage form such as a gel or a paste, for example, and is made into a dentifrice composition such as a toothpaste composition or a gel dentifrice composition, an oral composition for application, or the like. be able to.
本発明の口腔用組成物は、20℃における粘度が1000〜10000dPa・sであるものが好ましく、1500〜9000dPa・sであるものがより好ましく、2000〜8000dPa・sであるものがさらに好ましい。粘度を10000dPa・s以下とすることによって、未溶解状態の二糖類(A)により組成物の構造粘性を持たせつつ、含有される水(B)中のフッ素イオン供給化合物(C)のフッ素イオンの流動性を確保することができる。口腔用組成物の粘度は、粘度測定用の容器に詰め、20℃の恒温器で24時間保存した後、ヘリパス型粘度計(B型粘度計)を用いて、ロータH7、回転数2.5rpm、1分間の条件で測定することができる。 The oral composition of the present invention preferably has a viscosity of 1000 to 10,000 dPa · s at 20 ° C., more preferably 1500 to 9000 dPa · s, and still more preferably 2000 to 8000 dPa · s. By setting the viscosity to 10000 dPa · s or less, the fluorine ion of the fluorine ion supply compound (C) in the water (B) contained while giving the structural viscosity of the composition by the undissolved disaccharide (A) Can be ensured. The viscosity of the composition for oral cavity is packed in a container for viscosity measurement and stored in a thermostat at 20 ° C. for 24 hours. Then, using a helicopter type viscometer (B type viscometer), rotor H7, rotation speed 2.5 rpm Measurement can be performed under conditions of 1 minute.
以下、本発明について、実施例に基づき具体的に説明するが、本発明はこれら実施例に限定されるものではない。なお、以下の実施例において、%は質量%を意味する。 EXAMPLES Hereinafter, although this invention is demonstrated concretely based on an Example, this invention is not limited to these Examples. In the following examples,% means mass%.
(試験例1)
表1、表2に示すフッ素イオン供給化合物(フッ化ナトリウム)を含有する試料の各成分及びその含有量を混合して実施例1〜7、比較例1〜3の口腔用組成物(歯磨組成物)を調製した。なお、pHは中性(6〜8)であった。
(Test Example 1)
Compositions for oral cavity of Examples 1 to 7 and Comparative Examples 1 to 3 (dentifrice composition) by mixing each component of the sample containing the fluoride ion supply compound (sodium fluoride) shown in Table 1 and Table 2 and their contents Prepared). The pH was neutral (6-8).
実施例1〜7、比較例1〜3の歯磨組成物の各試料100mgをHAPペレット(APP−100 HOYA)10mm×10mm×2mmに塗布して3分間置いた後、イオン交換水で歯磨組成物を除去してペレットを乾燥させた。乾燥後のペレットから1Nの塩酸によって30秒間フッ素イオンの抽出を行い、フッ素イオン電極(ionplus-Fluoride(ORION社製))を用い、イオンアナライザー(Expandable ionAnalyzer EA 940(ORION社製))を使用してHAPペレットに吸着したフッ素量を定量した。
粘度の測定条件は、20℃の恒温器で1時間保存した後、ヘリパス粘度計(B型粘度計)でロータH7を用い、回転数2.5rpm、1分間である。
After applying 100 mg of each sample of the dentifrice compositions of Examples 1 to 7 and Comparative Examples 1 to 3 to HAP pellets (APP-100 HOYA) 10 mm × 10 mm × 2 mm and placing them for 3 minutes, the dentifrice composition with ion exchange water And the pellets were dried. Extraction of fluoride ions from the dried pellets with 1N hydrochloric acid for 30 seconds, using a fluorine ion electrode (ionplus-Fluoride (ORION)) and an ion analyzer (Expandable ionAnalyzer EA 940 (ORION)) The amount of fluorine adsorbed on the HAP pellet was quantified.
The viscosity was measured for 1 hour in a thermostat at 20 ° C., and then the rotor H7 was used with a helipath viscometer (B-type viscometer), and the rotation speed was 2.5 rpm and 1 minute.
表1に示すように、トレハロース(A)の少ない比較例1と、成分(A)と成分(B)の質量比(A/B)が1以上であるがトレハロースの含有量が25質量%よりも少ない比較例2とに比べて、トレハロース(A)を25〜45質量%含有し、水(B)に対する(A)の質量比(A/B)が1〜4である実施例1〜5は、いずれも高いフッ素取り込量が確認された。なお、比較例3は、成分(A)と水(B)の質量比(A/B)が4.8と大きいため、組成物が粉っぽくパサパサしており、粘度の測定ができなかった。また、ほぼ固形物であるため、フッ素取り込量を測定しなかった。 As shown in Table 1, the comparative example 1 with a small amount of trehalose (A) and the mass ratio (A / B) of the component (A) to the component (B) is 1 or more, but the trehalose content is more than 25% by mass. Compared with comparative example 2 with few, Examples 1-5 which contain 25-45 mass% of trehalose (A), and the mass ratio (A / B) of (A) to water (B) is 1-4. In each case, a high fluorine uptake was confirmed. In Comparative Example 3, since the mass ratio (A / B) of component (A) to water (B) was as large as 4.8, the composition was powdery and the viscosity could not be measured. . Moreover, since it was a substantially solid substance, the amount of fluorine uptake was not measured.
表2に示すように、トレハロースの含有量、水分量、粘度がほぼ等しい実施例6と実施例7の歯磨組成物であっても、エリスリトール、グリセリンを含有する実施例7は、実施例6よりもフッ素取り込量が増えており、トレハロース等の成分(A)にさらに(E)糖アルコール、及び/又はグリセリンを含有することによって、フッ素取り込量が向上することが確認された。 As shown in Table 2, even in the dentifrice compositions of Example 6 and Example 7 in which the trehalose content, water content, and viscosity are substantially equal, Example 7 containing erythritol and glycerin is more effective than Example 6. Further, it was confirmed that the fluorine uptake amount was improved by further containing (E) sugar alcohol and / or glycerin in the component (A) such as trehalose.
Claims (6)
(A)20℃における水に対する溶解度が50質量%以下である二糖類 25〜50質量%、
(B)水 10〜40質量%、及び
(C)フッ素イオン供給化合物 フッ素原子換算で0.002〜5質量%
を含有し、成分(A)と成分(B)の質量比(A/B)が1〜4である口腔用組成物。 The following components (A), (B) and (C):
(A) 25-50 mass% of disaccharides whose solubility in water at 20 ° C. is 50 mass% or less,
(B) Water 10 to 40% by mass, and (C) Fluorine ion supply compound 0.002 to 5% by mass in terms of fluorine atoms
The composition for oral cavity in which the mass ratio (A / B) of a component (A) and a component (B) is 1-4.
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JP2022537786A (en) * | 2019-06-28 | 2022-08-29 | ザ プロクター アンド ギャンブル カンパニー | Oral care composition containing stannous ions |
US11839672B2 (en) | 2019-06-28 | 2023-12-12 | The Procter & Gamble Company | Dentifrice compositions comprising tin ions |
US11839671B2 (en) | 2019-06-28 | 2023-12-12 | The Procter & Gamble Company | Oral care compositions comprising tin ions |
US12104021B2 (en) | 2021-02-22 | 2024-10-01 | The Procter & Gamble Company | Recycling of superabsorbent fibers with an extensional flow device |
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JP2022537786A (en) * | 2019-06-28 | 2022-08-29 | ザ プロクター アンド ギャンブル カンパニー | Oral care composition containing stannous ions |
JP7295281B2 (en) | 2019-06-28 | 2023-06-20 | ザ プロクター アンド ギャンブル カンパニー | Oral care composition containing stannous ions |
US11839672B2 (en) | 2019-06-28 | 2023-12-12 | The Procter & Gamble Company | Dentifrice compositions comprising tin ions |
US11839671B2 (en) | 2019-06-28 | 2023-12-12 | The Procter & Gamble Company | Oral care compositions comprising tin ions |
US12104021B2 (en) | 2021-02-22 | 2024-10-01 | The Procter & Gamble Company | Recycling of superabsorbent fibers with an extensional flow device |
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