JP4022286B2 - Oral composition - Google Patents
Oral composition Download PDFInfo
- Publication number
- JP4022286B2 JP4022286B2 JP18074897A JP18074897A JP4022286B2 JP 4022286 B2 JP4022286 B2 JP 4022286B2 JP 18074897 A JP18074897 A JP 18074897A JP 18074897 A JP18074897 A JP 18074897A JP 4022286 B2 JP4022286 B2 JP 4022286B2
- Authority
- JP
- Japan
- Prior art keywords
- sodium
- calcium carbonate
- composition
- flavor
- weight
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 33
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 46
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 23
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims description 20
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 claims description 20
- 235000014749 Mentha crispa Nutrition 0.000 claims description 14
- 244000246386 Mentha pulegium Species 0.000 claims description 14
- 235000016257 Mentha pulegium Nutrition 0.000 claims description 14
- 235000004357 Mentha x piperita Nutrition 0.000 claims description 14
- 235000001050 hortel pimenta Nutrition 0.000 claims description 14
- 229940011037 anethole Drugs 0.000 claims description 10
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 claims description 10
- 239000003205 fragrance Substances 0.000 claims description 8
- 210000000214 mouth Anatomy 0.000 claims description 6
- 229940087305 limonene Drugs 0.000 claims 2
- 244000078639 Mentha spicata Species 0.000 claims 1
- -1 terpene hydrocarbons Chemical class 0.000 description 23
- 239000000796 flavoring agent Substances 0.000 description 16
- 235000019634 flavors Nutrition 0.000 description 16
- 244000024873 Mentha crispa Species 0.000 description 13
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 229940034610 toothpaste Drugs 0.000 description 8
- 239000000606 toothpaste Substances 0.000 description 8
- 230000006866 deterioration Effects 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 238000007796 conventional method Methods 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 235000007586 terpenes Nutrition 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 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 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 229960003237 betaine Drugs 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
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 229940085605 saccharin sodium Drugs 0.000 description 3
- 108700004121 sarkosyl Proteins 0.000 description 3
- 150000003505 terpenes Chemical class 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229960003500 triclosan Drugs 0.000 description 3
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-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
- MPDGHEJMBKOTSU-YKLVYJNSSA-N 18beta-glycyrrhetic acid Chemical compound C([C@H]1C2=CC(=O)[C@H]34)[C@@](C)(C(O)=O)CC[C@]1(C)CC[C@@]2(C)[C@]4(C)CC[C@@H]1[C@]3(C)CC[C@H](O)C1(C)C MPDGHEJMBKOTSU-YKLVYJNSSA-N 0.000 description 2
- SVIJYLPSHPPVQF-UHFFFAOYSA-N 2-[2,2-diaminoethyl(dodecyl)amino]acetic acid Chemical compound CCCCCCCCCCCCN(CC(N)N)CC(O)=O SVIJYLPSHPPVQF-UHFFFAOYSA-N 0.000 description 2
- XGRSAFKZAGGXJV-UHFFFAOYSA-N 3-azaniumyl-3-cyclohexylpropanoate Chemical compound OC(=O)CC(N)C1CCCCC1 XGRSAFKZAGGXJV-UHFFFAOYSA-N 0.000 description 2
- IJALWSVNUBBQRA-UHFFFAOYSA-N 4-Isopropyl-3-methylphenol Chemical compound CC(C)C1=CC=C(O)C=C1C IJALWSVNUBBQRA-UHFFFAOYSA-N 0.000 description 2
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 2
- 239000011626 DL-alpha-tocopherylacetate Substances 0.000 description 2
- 235000001809 DL-alpha-tocopherylacetate Nutrition 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 235000019501 Lemon oil Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000010617 anise oil Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 239000001506 calcium phosphate 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
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N isopropylmethylphenol Natural products CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000010501 lemon oil Substances 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- 239000008368 mint flavor Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- 229960000414 sodium fluoride Drugs 0.000 description 2
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 229960004711 sodium monofluorophosphate Drugs 0.000 description 2
- 229940013618 stevioside Drugs 0.000 description 2
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 2
- 235000019202 steviosides Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- 229940042585 tocopherol acetate Drugs 0.000 description 2
- 239000000341 volatile oil Substances 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
- XMGQYMWWDOXHJM-SNVBAGLBSA-N (-)-α-limonene Chemical compound CC(=C)[C@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-SNVBAGLBSA-N 0.000 description 1
- QYIXCDOBOSTCEI-QCYZZNICSA-N (5alpha)-cholestan-3beta-ol Chemical compound C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CC1 QYIXCDOBOSTCEI-QCYZZNICSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- XPALGXXLALUMLE-UHFFFAOYSA-N 2-(dimethylamino)tetradecanoic acid Chemical compound CCCCCCCCCCCCC(N(C)C)C(O)=O XPALGXXLALUMLE-UHFFFAOYSA-N 0.000 description 1
- NGOZDSMNMIRDFP-UHFFFAOYSA-N 2-[methyl(tetradecanoyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCC(=O)N(C)CC(O)=O NGOZDSMNMIRDFP-UHFFFAOYSA-N 0.000 description 1
- HKKXJKUATKEWDT-UHFFFAOYSA-N 2-ethyl-2-(tetradecylamino)butanoic acid Chemical compound C(CCCCCCCCCCCCC)NC(C(=O)O)(CC)CC HKKXJKUATKEWDT-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- WBZFUFAFFUEMEI-UHFFFAOYSA-M Acesulfame k Chemical compound [K+].CC1=CC(=O)[N-]S(=O)(=O)O1 WBZFUFAFFUEMEI-UHFFFAOYSA-M 0.000 description 1
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- WJLVQTJZDCGNJN-UHFFFAOYSA-N Chlorhexidine hydrochloride Chemical compound Cl.Cl.C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 WJLVQTJZDCGNJN-UHFFFAOYSA-N 0.000 description 1
- IELOKBJPULMYRW-NJQVLOCASA-N D-alpha-Tocopheryl Acid Succinate Chemical compound OC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C IELOKBJPULMYRW-NJQVLOCASA-N 0.000 description 1
- 108010001682 Dextranase Proteins 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 101000925662 Enterobacteria phage PRD1 Endolysin Proteins 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- MPDGHEJMBKOTSU-UHFFFAOYSA-N Glycyrrhetinsaeure Natural products C12C(=O)C=C3C4CC(C)(C(O)=O)CCC4(C)CCC3(C)C1(C)CCC1C2(C)CCC(O)C1(C)C MPDGHEJMBKOTSU-UHFFFAOYSA-N 0.000 description 1
- 239000004378 Glycyrrhizin Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 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
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products 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-PICCSMPSSA-N 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N N-methylaminoacetic acid Natural products C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 108010077895 Sarcosine Proteins 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- MSCCTZZBYHQMQJ-AZAGJHQNSA-N Tocopheryl nicotinate Chemical compound C([C@@](OC1=C(C)C=2C)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)CC1=C(C)C=2OC(=O)C1=CC=CN=C1 MSCCTZZBYHQMQJ-AZAGJHQNSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010358 acesulfame potassium Nutrition 0.000 description 1
- 229960004998 acesulfame potassium Drugs 0.000 description 1
- 239000000619 acesulfame-K Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 229960000458 allantoin Drugs 0.000 description 1
- QYIXCDOBOSTCEI-UHFFFAOYSA-N alpha-cholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 QYIXCDOBOSTCEI-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
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Landscapes
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Description
【0001】
【発明が属する技術分野】
本発明は、多孔質炭酸カルシウム配合組成物におけるペパーミントおよびスペアミントの香味安定性を改善した口腔用組成物に関する。
【0002】
【従来の技術】
炭酸カルシウムからなる口腔用組成物においてペパーミントおよびスペアミントなどのミント系香料を配合する場合、経日安定性において香味の劣化およびすなわち酸化臭、土臭い、青臭いおよび苦み臭が発生し、併せて香調が変化することが知られている。それは、ミント系香料は主としてテルペン系炭化水素から構成されているが、多くの中に含有するテルペン系炭化水素 によるところが大きく、炭酸カルシウムとの親和性が高いため、経時的に成分の構成比率が変化することによる。従って、従来の炭酸カルシウムを研磨剤とする口腔用組成物は、香料の賦香率を高くすることにより香味の劣化、香味の変化を抑制していた。代表的な香料成分であるペパーミントおよびスペアミントには、テルペン系炭化水素を多く含有している。
【0003】
近年、低研磨性で高清掃機能を有する研磨剤として、炭酸化の方法により比表面積および吸油量を増加させた軽質炭酸カルシウム(特開平04−21518号、特開平09−20629号)が提案されている。しかしこの炭酸カルシウムは、高容積、高吸水性、高吸油性および高比表面積であるため口腔用組成物に配合する場合、従来の炭酸カルシウムとは異なり、単に賦香率を高めるだけでは、香味の劣化、香調の変化を抑制することは不可能であった。
【0004】
【発明が解決しようとする課題】
本発明の目的は、多孔質炭酸カルシウムを含有する口腔用組成物においてペパーミントおよびスペアミントを使用しても、香味の劣化および香調の変化のない口腔用組成物を提供することである。
【0005】
【発明を解決するための手段】
本発明者は、上記課題の解決のために、鋭意研究を重ねた結果、多孔質炭酸カルシウムを含有する口腔用組成物において、ある特定の香料成分すなわちd−リモネンおよび/又はアネトールを配合することにより、スペアミント、ペパーミントの香味の経日安定性が高まることを見出し、本発明を完成するに至った。すなわち、本発明はd−リモネンおよび/又はアネトールを配合して、スペアミント、ペパーミントの香味の安定性を改善した多孔質炭酸カルシウムを含有する口腔用組成物を提供することである。
【0006】
【発明の実施の形態】
本発明に用いる多孔質炭酸カルシウムは、化学合成された高純度軽質炭酸カルシウムであり、微粒子が連なった連鎖状粒子を多段階炭酸化行なうことにより得られるポーラスな炭酸カルシウムで、例えば、ポアカル−N(白石カルシウム社製)、IK−3000(白石中央研究所社製)として入手できる。本発明における、多孔質炭酸カルシウムの配合量は、0.1〜40重量%であり、0.5〜10重量%が好ましい。
本発明で用いるスペアミント、ペパーミントは市販の物を用いることができ、通常0.1〜5重量%、好ましくは0.5〜2重量%程度の割合で配合することができる。
【0007】
さらに、d−リモネンおよび/又はアネトールを配合する。これらは単品でも精油でも用いることができ、単品では合成、あるいは植物から精製したものを用い、また精油としては、d−リモネンを含有するレモン油、オレンジ油、アネトールを含有するアニス油などを用いることができる。これらは組成物全量に対して通常0.001〜1重量%、好ましくは0.01〜0.3重量%の割合で配合することができる。また、香料成分全量に対して通常0.1%〜20重量%、好ましくは0.5〜10重量%の割合で配合することができる。
【0008】
本発明の口腔用組成物は、常法により練歯磨、粉歯磨、軟膏剤、パスタ、などの形態に製造でき、特に練歯磨が実用上好ましい形態である。これら組成物はポリエチレン樹脂、ポリプロピレン樹脂等のポリオレフィン樹脂、、ポリエステル樹脂、ポリエチレンテルフタレ−ト樹脂、ポリカ−ボネ−ト樹脂、ポリスチレン樹脂、ポリアミド樹脂、ポリ塩化ビニル樹脂など通常に用いられる樹脂性の容器、例えば単層チュ−ブ、ラミネ−トチュ−ブなど何れにも充填し提供できる。
【0009】
また、本発明の口腔用組成物は上記の必須成分以外に、本発明の効果を損なわない範囲で公知の成分を適宜配合できる。
【0010】
例えば練歯磨の場合、研磨剤として、炭酸カルシウム、第2リン酸カルシウム、第3リン酸カルシウム、ヒドロキシアパタイト、ピロリン酸カルシウム、不溶性メタリン酸ナトリウム、酸化チタン、非晶質シリカ、結晶質シリカ、アルミノシリケート、酸化アルミニウム、水酸化アルミニウム、レジンなどを、単独または2種以上を組合わせて配合することができ、その配合量は、通常、組成物全量に対して10〜60重量%である。
【0011】
また発泡剤、洗浄剤としてのアニオン性界面活性剤は、アルキル硫酸ナトリウム、N−アシルザルコシン酸ナトリウム、N−アシルグルタミン酸塩から選ばれる1種または2種以上であり、特に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ン酸ナトリウム、N−ミリストイルザルコシン酸ナトリウム、N−パルミトイルグルタミン酸ナトリウムから選ばれる1種または2種以上であることが望ましい。これらの界面活性剤は、単独または2種以上を組み合わせて配合する。
【0012】
非イオン性界面活性剤としては、ショ糖脂肪酸エステル、マルトース脂肪酸エステル、ラクトース脂肪酸エステルなどの糖脂肪酸エステル、ポリオキシエチレンアルキルエーテル類、脂肪酸アルカノールアミド類、ポリオキシエチレンソルビタンモノラウレート、ポリオキシエチレンソルビタンモノステアレートなどのポリオキシエチレンソルビタン脂肪酸エステル、ポリオキシエチレン硬化ヒマシ油などのポリオキシエチレン脂肪酸エステル、ソルビタン脂肪酸エステル、脂肪酸モノグリセライドなどが挙げられる。
【0013】
両性イオン界面活性剤としては、N−ラウリルジアミノエチルグリシン、N−ミリスチルジエチルグリシンなどのN−アルキルジアミノエチルグリシン、N−アルキル−N−カルボキシメチルアンモニウムベタイン、2−アルキル−1−ヒドロキシエチルイミダゾリンベタインナトリウム、ラウリルジメチルアミノ酢酸ベタインなどが挙げられる。これらの界面活性剤は、単独または2種以上を組み合わせて配合する。通常、組成物全量に対して0.1〜10重量%である。
【0014】
湿潤剤としては、ソルビット、グリセリン、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、キシリット、マルチット、ラクチットなどを、単独または2種以上を組み合わせて配合することができる。その配合量は、通常、組成物全量に対して5〜70重量%である。
【0015】
pH調節剤としては、例えば、クエン酸、リン酸、リンゴ酸、ピロリン酸、乳酸、酒石酸、グリセロリン酸、酢酸、硝酸、ケイ酸、またはこれらの化学的に可能な塩や水酸化ナトリウムなどが挙げられ、これらは、組成物のpHが5〜9の範囲となるよう、単独または2種以上を組み合わせて配合することができる。その配合量は、通常、組成物全量に対して0.01〜2重量%である。
【0016】
増粘剤としては、例えば、セルロース誘導体が、カルボキシメチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース、ヒドロキシエチルセルロース、メチルセルロース、カルボキシメチルヒドロキシエチルセルロース、及びその塩類、カラゲナン、アルギン酸ナトリウム等のアルカリ金属アルギネート、キサンタンガム、トラガントガム、アラビアガム等のガム類、ポリビニルアルコール、ポリアクリル酸ナトリウム等の合成粘結剤、シリカゲル、アルミニウムシリカゲル、ビーガム等の無機粘結剤などを添加することも可能である。これら増粘剤の配合量は、通常、組成物全量に対して0.01〜5重量%である。
【0017】
さらに、本発明で用いるスペアミント、ペパーミント、d−リモネンおよびアネトール以外に、香味剤として、オイゲノール、サリチル酸メチル、チモール、l−リモネン、セージ油、ローズマリー油、珪皮油などを、単独または2種以上を組み合わせて、組成物全量に対して0.1〜5重量%、好ましくは0.5〜2重量%程度の割合で配合することができる。
【0018】
また、甘味剤として、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、ネオヘスペリジルジヒドロカルコン、グリチルリチン、ペリラルチン、タウマチン、アスパラチルフェニルアラニルメチルエステル、ρ−メトキシシンナミックアルデヒド、キシリットなどを、組成物全量に対して0.01〜1重量%、好ましくは0.05〜0.5重量%の割合で配合することができる。
【0019】
さらに、本発明の口腔用組成物には、水不溶性の非カチオン殺菌剤以外の薬効成分として、酢酸dl−α−トコフェロール、コハク酸トコフェロール、またはニコチン酸トコフェロールなどのビタミンE類、塩酸クロルヘキシジン、塩化セチルピリジニウム、塩化ベンゼトニウムなどのカチオン性殺菌剤、ドデシルジアミノエチルグリシンなどの両性殺菌剤、トリクロサン、イソプロピルメチルフェノールなどの非イオン性殺菌剤、デキストラナーゼ、アミラーゼ、プロテアーゼ、ムタナーゼ、リゾチーム、溶菌酵素(リテックエンザイム)などの酵素、モノフルオロリン酸ナトリウム、モノフルオロリン酸カリウムなどのアルカリ金属モノフルオロフォスフェート、フッ化ナトリウム、フッ化第一錫などのフッ化物、トラネキサム酸やイプシロンアミノカプロン酸、アルミニウムクロルヒドロキシルアラントイン、ジヒドロコレステロール、グリチルリチン塩類、グリチルレチン酸、グリセロフォスフェート、クロロフィル、塩化ナトリウム、カロペプタイド、水溶性無機リン酸化合物などを、単独または2種以上を組み合わせて配合することができる。
【0020】
【実施例】
以下、試験例および実施例により本発明をさらに詳しく説明するが、本発明はこれらの実施例に限定されるものではない。実施例中の配合量はいずれも重量%である。実施例
以下、試験例および実施例により本発明をさらに詳しく説明するが、本発明はこれらの実施例に限定されるものではない。実施例中の配合量はいずれも重量%である。
【0021】
[試験例]
表1に示す練歯磨を常法に従って調製してラミネートチューブに充填し、40℃にて3ヶ月保存した後のテルペンの香味の劣化および香味の変化を下記の基準で評価した。
【0022】
(香味の劣化および変化の評価基準)
香味の劣化
−・・・・・劣化なし
+・・・・・わずかに劣化
++・・・・・明らかに劣化
香味の変化
A・・・・・変化なし
B・・・・・酸化臭
C・・・・・青臭
D・・・・・苦み臭
【0023】
【表1】
【0024】
表1の結果から明らかなごとく、比較例に比べ、多孔質炭酸カルシウムおよびd−リモネン および/又はアネトールを配合した実施例ではペパーミントおよびスペアミントにおける、香味の経日安定性の改善が認められる。
【0025】
〔実施例8〕
下記の各成分を常法に従って練歯磨を調製し、上記と同様のラミネートチューブに充填した。
成分 配合量(%)
多孔質炭酸カルシウム 30.0
炭酸カルシウム 5.0
ソルビット 20.0
キシリット 5.0
カラギーナン 1.5
ラウリル硫酸ナトリウム 0.15
N−ラウロイルザルコシン酸ナトリウム 1.0
サッカリンナトリウム 1.0
トリクロサン 0.1
アニス油 0.1
ペパーミント系香料 1.0
精製水 残部
合計 100.0
【0026】
〔実施例9〕
下記の各成分を常法に従って練歯磨を調製し、上記と同様のラミネートチューブに充填した。
成分 配合量(%)
多孔質炭酸カルシウム 6.0
炭酸カルシウム 25.0
ソルビット 20.0
プロピレングリコール 5.0
ヒドロキシエチルセルロースナトリウム 1.5
N−ラウロイルザルコシン酸ナトリウム 1.5
ステビオサイド 0.5
モノフルオロリン酸ナトリウム 0.2
イソプロピルメチルフェノール 0.5
ポリオキシエチレン(200)ポリオキシ
プロピレン(70)ブロックコポリマー 1.0
レモン油 0.1
スペアミント 1.0
精製水 残部
合計 100.0
【0027】
〔実施例10〕
下記の各成分を常法に従って練歯磨を調製し、上記と同様のポンプ式ディスペンサーラミネートチューブに充填した。
成分 配合量(%)
多孔質炭酸カルシウム 20.0
ソルビット 20.0
グリセリン 5.0
アルギン酸ナトリウム 1.5
N−ミリストイルザルコシン酸ナトリウム 0.5
サッカリンナトリウム 0.1
トリクロサン 0.2
フッ化ナトリウム 0.2
酢酸dl−α−トコフェロール 0.5
ポリオキシエチレン(150)ポリオキシ
プロピレン(35)ブロックコポリマー 1.0
スペアミント 0.2
ペパーミント 1.0
d−リモネン 0.1
アネトール 0.01
精製水 残部
合計 100.0
以上実施例8〜10により調製した口腔用組成物においても、スペアミント、ペパーミントミント系香料の香味安定性を改善した。
【0028】
【発明の効果】
本発明によれば、多孔質炭酸カルシウムを含有する口腔用組成物において、d−リモネンおよび/又はアネトールを配合することによって、スペアミント、ペパーミントの香味の経日安定性を高めた口腔用組成物が得られる。[0001]
[Technical field to which the invention belongs]
The present invention relates to an oral composition having improved flavor stability of peppermint and spearmint in a porous calcium carbonate-containing composition.
[0002]
[Prior art]
When blending mint flavors such as peppermint and spearmint in a composition for oral cavity made of calcium carbonate, the deterioration of flavor and the odor, earthy smell, blue odor and bitter odor occur in the stability over time, and the fragrance tone is also added. It is known to change. This is because mint-based fragrances are mainly composed of terpene-based hydrocarbons, but many of them are terpene-based hydrocarbons. This is largely due to the fact that the component ratio of the components changes over time because of its high affinity with calcium carbonate. Therefore, the composition for oral cavity which uses the conventional calcium carbonate as an abrasive | polishing agent suppressed the deterioration of flavor and the change of flavor by making the fragrance | flavor perfume high. Peppermint and spearmint, which are typical perfume ingredients, contain a large amount of terpene hydrocarbons.
[0003]
In recent years, light calcium carbonate (JP 04-21518, JP 09-20629) having a specific surface area and oil absorption increased by a carbonation method has been proposed as an abrasive having low polishing properties and a high cleaning function. ing. However, this calcium carbonate has a high volume, high water absorption, high oil absorption, and high specific surface area, so when blended into an oral composition, it is different from conventional calcium carbonate by simply increasing the flavoring rate. It was impossible to suppress the deterioration of fragrance and the change of fragrance.
[0004]
[Problems to be solved by the invention]
An object of the present invention is to provide an oral composition that does not deteriorate in flavor and change in flavor even when peppermint and spearmint are used in an oral composition containing porous calcium carbonate.
[0005]
[Means for Solving the Invention]
As a result of intensive studies to solve the above problems, the present inventor formulated a specific perfume ingredient, that is, d-limonene and / or anethole in an oral composition containing porous calcium carbonate. As a result, it was found that the daily stability of the flavor of spearmint and peppermint is increased, and the present invention has been completed. That is, this invention is providing the composition for oral cavity containing the porous calcium carbonate which mix | blended d-limonene and / or anethole and improved the stability of the flavor of spearmint and peppermint.
[0006]
DETAILED DESCRIPTION OF THE INVENTION
The porous calcium carbonate used in the present invention is chemically synthesized high-purity light calcium carbonate, and is porous calcium carbonate obtained by performing multi-stage carbonation of chain-like particles in which fine particles are connected. For example, Porecal-N (Manufactured by Shiraishi Calcium Co., Ltd.) and IK-3000 (manufactured by Shiroishi Central Research Laboratories). The compounding quantity of the porous calcium carbonate in this invention is 0.1 to 40 weight%, and 0.5 to 10 weight% is preferable.
As the spearmint and peppermint used in the present invention, commercially available products can be used, and they can usually be blended at a ratio of about 0.1 to 5% by weight, preferably about 0.5 to 2% by weight.
[0007]
Furthermore, d-limonene and / or anethole is blended. These can be used either individually or as essential oils, and as a single product, those synthesized or purified from plants are used, and as essential oils, lemon oil containing d-limonene, orange oil, anise oil containing anethole, etc. are used. be able to. These can be blended in a proportion of usually 0.001 to 1% by weight, preferably 0.01 to 0.3% by weight, based on the total amount of the composition. Moreover, it can mix | blend in the ratio of 0.1 to 20 weight% normally with respect to the fragrance | flavor component whole quantity, Preferably it is 0.5 to 10 weight%.
[0008]
The composition for oral cavity of the present invention can be produced in the form of toothpaste, powder toothpaste, ointment, pasta and the like by a conventional method, and toothpaste is a practically preferable form. These compositions include polyolefin resins such as polyethylene resins and polypropylene resins, polyester resins, polyethylene terephthalate resins, polycarbonate resins, polystyrene resins, polyamide resins, and polyvinyl chloride resins. Any container such as a single layer tube or a laminar tube can be filled and provided.
[0009]
Moreover, the composition for oral cavity of this invention can mix | blend well-known components suitably in the range which does not impair the effect of this invention other than said essential component.
[0010]
For example, in the case of toothpaste, as an abrasive, calcium carbonate, dicalcium phosphate, tricalcium phosphate, hydroxyapatite, calcium pyrophosphate, insoluble sodium metaphosphate, titanium oxide, amorphous silica, crystalline silica, aluminosilicate, aluminum oxide, Aluminum hydroxide, resin and the like can be blended alone or in combination of two or more, and the blending amount is usually 10 to 60% by weight based on the total amount of the composition.
[0011]
Further, the anionic surfactant as a foaming agent or a cleaning agent is one or more selected from sodium alkyl sulfate, sodium N-acyl sarcosine, and N-acyl glutamate, and particularly sodium lauryl sulfate and sodium myristyl sulfate. , N-lauroyl sarcosinate sodium, N-myristoyl sarcosine sodium salt, N-palmitoyl glutamate sodium salt is preferably one or more. These surfactants are blended alone or in combination of two or more.
[0012]
Nonionic surfactants include sugar fatty acid esters such as sucrose fatty acid ester, maltose fatty acid ester, lactose fatty acid ester, polyoxyethylene alkyl ethers, fatty acid alkanolamides, polyoxyethylene sorbitan monolaurate, polyoxyethylene Examples include polyoxyethylene sorbitan fatty acid esters such as sorbitan monostearate, polyoxyethylene fatty acid esters such as polyoxyethylene hydrogenated castor oil, sorbitan fatty acid esters, and fatty acid monoglycerides.
[0013]
Examples of zwitterionic surfactants include N-alkyldiaminoethylglycine such as N-lauryldiaminoethylglycine and N-myristyldiethylglycine, N-alkyl-N-carboxymethylammonium betaine, 2-alkyl-1-hydroxyethylimidazoline betaine Sodium, lauryldimethylaminoacetic acid betaine, etc. are mentioned. These surfactants are blended alone or in combination of two or more . Usually, it is 0.1 to 10% by weight based on the total amount of the composition.
[0014]
As the wetting agent, sorbit, glycerin, ethylene glycol, propylene glycol, 1,3-butylene glycol, polyethylene glycol, polypropylene glycol, xylite, maltite, lactit and the like can be used alone or in combination of two or more. The amount is usually 5 to 70% by weight based on the total amount of the composition.
[0015]
Examples of the pH adjuster include citric acid, phosphoric acid, malic acid, pyrophosphoric acid, lactic acid, tartaric acid, glycerophosphoric acid, acetic acid, nitric acid, silicic acid, or a chemically possible salt or sodium hydroxide thereof. These can be blended alone or in combination of two or more so that the pH of the composition is in the range of 5-9. The compounding quantity is 0.01 to 2 weight% normally with respect to the composition whole quantity.
[0016]
Examples of the thickener include cellulose derivatives such as carboxymethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxyethylcellulose, methylcellulose, carboxymethylhydroxyethylcellulose, and salts thereof, carrageenan, alkali metal alginates such as sodium alginate, xanthan gum, and tragacanth gum. It is also possible to add gums such as gum arabic, synthetic binders such as polyvinyl alcohol and sodium polyacrylate, and inorganic binders such as silica gel, aluminum silica gel and bee gum. The amount of these thickeners is usually 0.01 to 5% by weight based on the total amount of the composition.
[0017]
Further, in addition to spearmint, peppermint, d-limonene and anethole used in the present invention, eugenol, methyl salicylate, thymol, l-limonene, sage oil, rosemary oil, cinnamon oil, etc., alone or in combination By combining the above, it can be blended at a ratio of 0.1 to 5% by weight, preferably about 0.5 to 2% by weight, based on the total amount of the composition.
[0018]
As sweeteners, saccharin sodium, acesulfame potassium, stevioside, neohesperidyl dihydrochalcone, glycyrrhizin, perilartine, thaumatin, asparatylphenylalanyl methyl ester, ρ-methoxycinnamic aldehyde, xylit, etc. in the total amount of the composition It can be blended at a ratio of 0.01 to 1% by weight, preferably 0.05 to 0.5% by weight.
[0019]
Furthermore, in the oral composition of the present invention, vitamin Es such as dl-α-tocopherol acetate, tocopherol succinate, or tocopherol nicotinate, chlorhexidine hydrochloride, chlorinated chloride as medicinal ingredients other than water-insoluble non-cationic fungicides Cationic fungicides such as cetylpyridinium and benzethonium chloride, amphoteric fungicides such as dodecyldiaminoethylglycine, nonionic fungicides such as triclosan and isopropylmethylphenol, dextranase, amylase, protease, mutanase, lysozyme, lytic enzyme ( Retech enzyme), alkali metal monofluorophosphates such as sodium monofluorophosphate and potassium monofluorophosphate, fluorides such as sodium fluoride and stannous fluoride, tranexamic acid and ip Long aminocaproic acid, aluminum chlorohydroxyl allantoin, dihydrocholesterol, glycyrrhizin salts, glycyrrhetinic acid, glycerophosphate, chlorophyll, sodium chloride, caropeptide, water-soluble inorganic phosphate compound, etc. may be used alone or in combination of two or more. it can.
[0020]
【Example】
EXAMPLES Hereinafter, although a test example and an Example demonstrate this invention further in detail, this invention is not limited to these Examples. The blending amounts in the examples are all by weight. EXAMPLES Hereinafter, the present invention will be described in more detail with reference to test examples and examples, but the present invention is not limited to these examples. The blending amounts in the examples are all by weight.
[0021]
[Test example]
Toothpaste shown in Table 1 were prepared according to a conventional method and filled into laminated tubes, the 3-month deterioration and change of fragrance taste flavor terpene after storage at 40 ° C. was evaluated according to the following criteria.
[0022]
(Evaluation criteria for flavor deterioration and changes)
Deterioration of flavor-No deterioration + ... Slightly deteriorated ++ ... Clearly deteriorated
Change in flavor A ... No change B ... Oxidized odor C ... Blue odor D ... Bitter odor [0023]
[Table 1]
[0024]
As is apparent from the results in Table 1, porous calcium carbonate and d-limonene were compared to the comparative example. In the examples blended with and / or anethole, an improvement in the daily stability of flavor is observed in peppermint and spearmint.
[0025]
[Example 8 ]
A toothpaste was prepared in accordance with a conventional method for each of the following components, and filled in a laminate tube similar to the above.
Ingredient Amount (%)
Porous calcium carbonate 30.0
Calcium carbonate 5.0
Sorbit 20.0
Xylit 5.0
Carrageenan 1.5
Sodium lauryl sulfate 0.15
Sodium N-lauroyl sarcosinate 1.0
Saccharin sodium 1.0
Triclosan 0.1
Anise oil 0.1
Peppermint flavoring 1.0
Purified water balance Total 100.0
[0026]
[Example 9 ]
A toothpaste was prepared in accordance with a conventional method for each of the following components, and filled in a laminate tube similar to the above.
Ingredient Amount (%)
Porous calcium carbonate 6.0
Calcium carbonate 25.0
Sorbit 20.0
Propylene glycol 5.0
Hydroxyethylcellulose sodium 1.5
Sodium N-lauroyl sarcosinate 1.5
Stevioside 0.5
Sodium monofluorophosphate 0.2
Isopropylmethylphenol 0.5
Polyoxyethylene (200) polyoxypropylene (70) block copolymer 1.0
Lemon oil 0.1
Spearmint 1.0
Purified water balance Total 100.0
[0027]
[Example 1 0 ]
A toothpaste was prepared according to a conventional method from the following components, and filled in a pump-type dispenser laminate tube similar to the above.
Ingredient Amount (%)
Porous calcium carbonate 20.0
Sorbit 20.0
Glycerin 5.0
Sodium alginate 1.5
Sodium N-myristoyl sarcosinate 0.5
Saccharin sodium 0.1
Triclosan 0.2
Sodium fluoride 0.2
Dl-α-tocopherol acetate 0.5
Polyoxyethylene (150) polyoxypropylene (35) block copolymer 1.0
Spearmint 0.2
Peppermint 1.0
d-limonene 0.1
Anethole 0.01
Purified water balance Total 100.0
In the oral compositions prepared according to Examples 8 to 10 as described above, the flavor stability of spearmint and peppermint mint flavors was improved.
[0028]
【The invention's effect】
According to the present invention, there is provided an oral composition containing a porous calcium carbonate, wherein d-limonene and / or anethole is mixed to improve the daily stability of the flavor of spearmint and peppermint. can get.
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18074897A JP4022286B2 (en) | 1997-06-19 | 1997-06-19 | Oral composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18074897A JP4022286B2 (en) | 1997-06-19 | 1997-06-19 | Oral composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1112145A JPH1112145A (en) | 1999-01-19 |
| JP4022286B2 true JP4022286B2 (en) | 2007-12-12 |
Family
ID=16088635
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18074897A Expired - Lifetime JP4022286B2 (en) | 1997-06-19 | 1997-06-19 | Oral composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4022286B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3422262B2 (en) * | 1998-08-28 | 2003-06-30 | 株式会社島津製作所 | Sample cooling device |
| EP1536749A2 (en) * | 2002-07-08 | 2005-06-08 | Joe S. Wilkins, Jr. | Antibacterial formulations |
| AU2010363052B2 (en) * | 2010-10-27 | 2014-11-20 | Colgate-Palmolive Company | Oral care composition comprising arginine and calcium carbonate |
| JP6007696B2 (en) * | 2012-09-19 | 2016-10-12 | ライオン株式会社 | Dentifrice composition and method for producing the same |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52125639A (en) * | 1976-04-12 | 1977-10-21 | Sunstar Inc | Compound of dentifrice without saccharin |
| JPS5426339A (en) * | 1977-07-28 | 1979-02-27 | Lion Dentifrice Co Ltd | Oral cavity treating composition |
| JPS62155207A (en) * | 1985-12-27 | 1987-07-10 | Lion Corp | Oral composition |
| JPH0597639A (en) * | 1991-10-08 | 1993-04-20 | Lion Corp | Composition for oral cavity |
| JPH08301743A (en) * | 1995-04-28 | 1996-11-19 | Sunstar Inc | Dentifrice composition |
| JP2981595B2 (en) * | 1995-07-04 | 1999-11-22 | 株式会社白石中央研究所 | Sterile calcium carbonate composition, aqueous suspension composition thereof and methods for producing them |
-
1997
- 1997-06-19 JP JP18074897A patent/JP4022286B2/en not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| JPH1112145A (en) | 1999-01-19 |
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