JPH07304641A - Tooth paste composition and its production - Google Patents
Tooth paste composition and its productionInfo
- Publication number
- JPH07304641A JPH07304641A JP12066394A JP12066394A JPH07304641A JP H07304641 A JPH07304641 A JP H07304641A JP 12066394 A JP12066394 A JP 12066394A JP 12066394 A JP12066394 A JP 12066394A JP H07304641 A JPH07304641 A JP H07304641A
- Authority
- JP
- Japan
- Prior art keywords
- dentifrice composition
- silica
- polyhydric alcohol
- viscosity
- water
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 238000004519 manufacturing process Methods 0.000 title claims description 19
- 239000000606 toothpaste Substances 0.000 title abstract description 7
- 229940034610 toothpaste Drugs 0.000 title abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 23
- 238000002156 mixing Methods 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 17
- 239000004359 castor oil Substances 0.000 claims abstract description 15
- 235000019438 castor oil Nutrition 0.000 claims abstract description 15
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims abstract description 15
- 238000004438 BET method Methods 0.000 claims abstract description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000551 dentifrice Substances 0.000 claims description 22
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 14
- -1 polyoxyethylene Polymers 0.000 claims description 14
- 229910021485 fumed silica Inorganic materials 0.000 claims description 9
- 230000014759 maintenance of location Effects 0.000 abstract description 9
- 238000000926 separation method Methods 0.000 abstract description 7
- 239000007788 liquid Substances 0.000 abstract description 4
- 239000003921 oil Substances 0.000 abstract 1
- 238000011156 evaluation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 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 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000003082 abrasive agent Substances 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
- 239000000654 additive Substances 0.000 description 2
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 2
- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 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
- 239000002304 perfume Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229940085605 saccharin sodium Drugs 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-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
- XGRSAFKZAGGXJV-UHFFFAOYSA-N 3-azaniumyl-3-cyclohexylpropanoate Chemical compound OC(=O)CC(N)C1CCCCC1 XGRSAFKZAGGXJV-UHFFFAOYSA-N 0.000 description 1
- AXCXHFKZHDEKTP-NSCUHMNNSA-N 4-methoxycinnamaldehyde Chemical compound COC1=CC=C(\C=C\C=O)C=C1 AXCXHFKZHDEKTP-NSCUHMNNSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 108010001682 Dextranase Proteins 0.000 description 1
- 239000004378 Glycyrrhizin Substances 0.000 description 1
- BIVBRWYINDPWKA-VLQRKCJKSA-L Glycyrrhizinate dipotassium Chemical compound [K+].[K+].O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@H]1CC[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@](C)(CC[C@@]5(CC[C@@]4(C)[C@]3(C)CC[C@H]2C1(C)C)C)C(O)=O)C([O-])=O)[C@@H]1O[C@H](C([O-])=O)[C@@H](O)[C@H](O)[C@H]1O BIVBRWYINDPWKA-VLQRKCJKSA-L 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 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 1
- 235000014749 Mentha crispa Nutrition 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 244000078639 Mentha spicata Species 0.000 description 1
- 235000004357 Mentha x piperita 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
- XCOJIVIDDFTHGB-UEUZTHOGSA-N Perillartine Chemical compound CC(=C)[C@H]1CCC(\C=N\O)=CC1 XCOJIVIDDFTHGB-UEUZTHOGSA-N 0.000 description 1
- 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 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229960000458 allantoin Drugs 0.000 description 1
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-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
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 229940011037 anethole Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229920003064 carboxyethyl cellulose Polymers 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- QGGZBXOADPVUPN-UHFFFAOYSA-N dihydrochalcone Chemical compound C=1C=CC=CC=1C(=O)CCC1=CC=CC=C1 QGGZBXOADPVUPN-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 229940101029 dipotassium glycyrrhizinate Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 108010000165 exo-1,3-alpha-glucanase Proteins 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
- 229960004949 glycyrrhizic acid Drugs 0.000 description 1
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
- 235000019410 glycyrrhizin Nutrition 0.000 description 1
- 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 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- AXCXHFKZHDEKTP-UHFFFAOYSA-N para-methoxycinnamaldehyde Natural products COC1=CC=C(C=CC=O)C=C1 AXCXHFKZHDEKTP-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 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
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 229960004711 sodium monofluorophosphate Drugs 0.000 description 1
- 229940013618 stevioside Drugs 0.000 description 1
- 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 1
- 235000019202 steviosides Nutrition 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 235000010436 thaumatin Nutrition 0.000 description 1
- 239000000892 thaumatin Substances 0.000 description 1
- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
- 229960000401 tranexamic acid Drugs 0.000 description 1
- 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 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 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 1
- 229930007845 β-thujaplicin Natural products 0.000 description 1
Landscapes
- Cosmetics (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は歯磨組成物およびその製
造方法、さらに詳しくは経日で粘度変化の少なく、保型
性の良好な歯磨組成物およびその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a dentifrice composition and a method for producing the same, and more particularly to a dentifrice composition which exhibits little change in viscosity over time and has good shape retention, and a method for producing the same.
【0002】[0002]
【従来の技術及び解決しようとする課題】歯磨組成物に
用いられる研磨剤として、炭酸カルシウム、リン酸カル
シウム、水酸化アルミニウム、シリカ等が広く用いられ
ているが、最近では透明感のある剤型や軽い使用感が得
られるシリカ系研磨剤の需要が高まってきている。その
中でも、火成性シリカは吸水性が高く、保型性が良好で
あるという特徴が挙げられ、歯磨組成物の使用感を良好
にするために火成性シリカが用いられる。火成性シリカ
を配合することにより保型性を良好にした歯磨組成物の
技術としては特開昭60−75412号で開示された
り、また、火成性シリカとポリエチレングリコールを配
合した口腔用組成物が特開昭63−162617で開示
されている。しかしながら、我々の検討ではこれらの技
術では火成性シリカを使用することにより、製造直後か
ら時間が経過するにつれて、急激な粘度上昇変化が起こ
るという問題があることがわかった。このため、製造直
後では粘度が低すぎ、また経日で粘度が高くなりすぎる
とチューブから絞りだしにくくなったり、固液分離が生
じる傾向があるなど不都合な点が生じ、品質管理を行な
うことが難しくなる。以上のことから、火成性シリカを
歯磨組成物に配合する際、経日粘度変化について改善の
余地があると考える。2. Description of the Related Art Calcium carbonate, calcium phosphate, aluminum hydroxide, silica, etc. are widely used as abrasives used in dentifrice compositions, but recently, they have a transparent formulation and a light weight. There is an increasing demand for silica-based abrasives that provide a feeling of use. Among them, the igneous silica has a feature that it has a high water absorption and a good shape retention property, and the ignitable silica is used for improving the feeling of use of the dentifrice composition. As a technique of a dentifrice composition having good shape retention by blending a pyrogenic silica, it is disclosed in JP-A-60-75412, and an oral composition containing a blend of a pyrogenic silica and polyethylene glycol. The product is disclosed in JP-A-63-162617. However, in our study, it has been found that these techniques have a problem that the use of the fumed silica causes a rapid change in the viscosity with the passage of time immediately after the production. For this reason, if the viscosity is too low immediately after production, or becomes too high over time, it becomes difficult to squeeze out of the tube, and solid-liquid separation tends to occur, which causes inconveniences and quality control can be performed. It gets harder. From the above, it is considered that there is room for improvement in the viscosity change with time when the ignitable silica is blended in the dentifrice composition.
【0003】[0003]
【課題を解決するための手段】本発明者らは火成性シリ
カを配合する歯磨組成物の経日粘度変化の改善について
鋭意研究を行なった結果、ポリオキシエチレン硬化ヒマ
シ油および、特定比率の多価アルコール/水を配合する
ことにより、経日での粘度変化が少なく、液分離のない
安定な歯磨組成物が得られることを見出した。またその
製造方法についても知見が得られ、本発明を完成するに
至った。Means for Solving the Problems The inventors of the present invention have conducted diligent research on the improvement of the daily viscosity change of a dentifrice composition containing ignitable silica. As a result, polyoxyethylene hydrogenated castor oil and a specific ratio of It has been found that by adding a polyhydric alcohol / water, it is possible to obtain a stable dentifrice composition with little viscosity change over time and without liquid separation. Further, knowledge has been obtained regarding the manufacturing method thereof, and the present invention has been completed.
【0004】本発明は、歯磨組成物において、火成性シ
リカにポリオキシエチレン硬化ヒマシ油、さらに特定比
率の多価アルコール/水を配合してなることを特徴とす
る口腔用組成物を提供するものである。The present invention provides a dentifrice composition, which is characterized by comprising a polyoxyethylene hydrogenated castor oil and a polyhydric alcohol / water in a specific ratio in the ignitable silica. It is a thing.
【0005】また本発明は、ポリオキシエチレン硬化ヒ
マシ油を多価アルコール/水系溶液中に混合した後、火
成性シリカを混合することを特徴とする歯磨組成物の製
造方法を提供するものである。The present invention also provides a method for producing a dentifrice composition, which comprises mixing polyoxyethylene hydrogenated castor oil in a polyhydric alcohol / water-based solution and then mixing ignitable silica. is there.
【0006】本発明で用いられる湿潤剤として、ソルビ
ット、プロピレングリコール、グリセリン、ポリエチレ
ングリコールなどの多価アルコールが用いられる。これ
らは多価アルコールと水との比率が1:1.4〜1:
2.2になるよう配合した場合が最も好ましい。水の比
率が1.4未満であると、経日で粘度が上昇し、2.2
をこえると分離が生じる。また多価アルコールの配合量
としては、好ましくは通常25〜40重量%配合でき
る。25重量%未満であると保型性が不良となり、外観
が損なわれる恐れがあり、また40重量%をこえると使
用感が低下する。As the wetting agent used in the present invention, polyhydric alcohols such as sorbit, propylene glycol, glycerin and polyethylene glycol are used. These have a ratio of polyhydric alcohol to water of 1: 1.4 to 1:
It is most preferable that the compounding ratio is 2.2. If the ratio of water is less than 1.4, the viscosity will increase with the lapse of time, resulting in 2.2.
If it exceeds, separation will occur. The polyhydric alcohol content is preferably 25 to 40% by weight. If the amount is less than 25% by weight, the shape retention may be poor and the appearance may be impaired, and if it exceeds 40% by weight, the usability may be deteriorated.
【0007】本発明で用いられるポリオキシエチレン硬
化ヒマシ油としては酸化エチレンの平均付加モル数が4
0〜80のものが好ましく、特に60モルであるものが
好ましい。また、配合量は0.1〜2重量%であり、好
ましくは0.2〜0.8%が好ましい。ポリオキシエチ
レン硬化ヒマシ油の配合量が0.1%未満であると粘度
変化が大きく、また2重量%をこえるとポリオキシエチ
レン硬化ヒマシ油の有する油っぽさが生じるので使用感
が不良になるという問題がある。The polyoxyethylene hydrogenated castor oil used in the present invention has an average added mole number of ethylene oxide of 4
It is preferably from 0 to 80, particularly preferably from 60 mol. The blending amount is 0.1 to 2% by weight, preferably 0.2 to 0.8%. If the content of polyoxyethylene hydrogenated castor oil is less than 0.1%, there will be a large change in viscosity, and if it exceeds 2% by weight, the polyoxyethylene hydrogenated castor oil will have an oily feel, resulting in a poor feeling in use. There is a problem of becoming.
【0008】本発明で用いられる火成性シリカとしては
種々選択されるが、その中でも特に比表面積(BET
法)が175〜225m2/gのものが好ましい。比表
面積が175m2/g以下であると、保型性に劣り、2
25m2/g以上であると経日で粘度が上昇し、容器か
ら絞り出しにくくなる。このましい火成性シリカとして
はデグサ社製のAerosil 、徳山曹達社製のレオ
ロシール QS−20等が挙げられる。火成性シリカは
通常1〜4%配合、より好ましくは2〜3%配合するこ
とが望ましい。1%以下であると保型性に劣り、4%以
上であると経日で粘度が上昇し、容器から絞り出しにく
くなる。また、火成性シリカは沈降性シリカと併用して
もよく、比表面積(BET法)500m2/g以下、よ
り好ましくは300m2/g以下のものが好ましい。具
体的には、Huber社Zeo49、Zeodent1
13、W,R,Grace社のSyloid AL−
1、63、74、404等が挙げられ、これらの1種ま
たは2種以上を配合し得るが、その配合量は1〜20%
配合、より好ましくは5〜15%配合することが好まし
い。[0008] The pyrogenic silica used in the present invention is selected variously, and among them, the specific surface area (BET) is particularly preferable.
Method) is preferably 175 to 225 m 2 / g. When the specific surface area is 175 m 2 / g or less, the shape retention is poor and 2
If it is at least 25 m 2 / g, the viscosity will increase with time and it will be difficult to squeeze out of the container. Examples of the preferable igneous silica include Aerosil manufactured by Degussa, and Reolosil QS-20 manufactured by Tokuyama Soda. It is desirable that the ignitable silica is usually added in an amount of 1 to 4%, more preferably 2 to 3%. If it is 1% or less, the shape retention is poor, and if it is 4% or more, the viscosity increases over time, and it becomes difficult to squeeze out from the container. Further, the ignitable silica may be used in combination with the precipitated silica, and the one having a specific surface area (BET method) of 500 m 2 / g or less, more preferably 300 m 2 / g or less is preferred. Specifically, Huber's Zeo49, Zeodent1
13, W, R, Syloid AL of Grace
1, 63, 74, 404, etc., and one or more of these may be blended, but the blending amount is 1 to 20%.
It is preferable to mix, more preferably 5 to 15%.
【0009】また、この歯磨組成物の製造方法として、
多価アルコール/水系溶液中にポリオキシエチレン硬化
ヒマシ油を混合させた後、火成性シリカを配合すると、
経日で粘度変化がより少なく、保型性の良好なものが得
られる。火成性シリカを配合する前にポリオキシエチレ
ン硬化ヒマシ油を多価アルコール/水系溶液中に混合さ
せない場合は、その効果は小さくなってしまう。Further, as a method for producing this dentifrice composition,
After mixing polyoxyethylene hydrogenated castor oil in a polyhydric alcohol / water-based solution, and then blending pyrogenic silica,
It is possible to obtain a product having less change in viscosity over time and good shape retention. If the polyoxyethylene hydrogenated castor oil is not mixed into the polyhydric alcohol / water solution before blending the fumed silica, the effect will be diminished.
【0010】本発明の歯磨組成物は常法に従って練歯磨
などの剤型にすることができ、必要に応じて適宜な成
分、例えばペパーミント、スペアミント等の精油、l−
メントール、カルボン、アネトール等の香料素材等の香
料、サッカリンナトリウム、ステビオサイド、ネオヘス
ピリジルヒドロカルコン、グリチルリチン、ソーマチ
ン、ペリラルチン、P−メトキシシンナミックアルデヒ
ド等の甘味剤、カルボキシエチルセルロースナトリウ
ム、カラギーナン、キサンタンガム、アルギン酸ナトリ
ウム、ヒドロキシエチルセルロース等の粘結剤、および
フッ化ナトリウム、モノフルオルリン酸ナトリウム、デ
キストラナーゼ、ムタナーゼ、ヒノキチオール、リゾチ
ーム、アラントイン、グリチルリチン酸ジカリウム、イ
プシロンアミノカプロン酸、トラネキサム酸、ビタミン
E及びその誘導体、塩化ナトリウム、アズレン等の有効
成分を本発明の効果を損なわない範囲で配合することが
できる。The dentifrice composition of the present invention can be made into a dosage form such as a toothpaste according to a conventional method, and if necessary, appropriate components such as essential oils such as peppermint and spearmint, 1-
Fragrances such as menthol, carvone, anethole, and other flavoring materials, sweeteners such as sodium saccharin, stevioside, neohespiridyl hydrochalcone, glycyrrhizin, thaumatin, perillartine, P-methoxycinnamic aldehyde, sodium carboxyethyl cellulose, carrageenan, xanthan gum, sodium alginate. , A binder such as hydroxyethyl cellulose, and sodium fluoride, sodium monofluorophosphate, dextranase, mutanase, hinokitiol, lysozyme, allantoin, dipotassium glycyrrhizinate, epsilon aminocaproic acid, tranexamic acid, vitamin E and its derivatives, Active ingredients such as sodium chloride and azulene can be added within a range that does not impair the effects of the present invention.
【0011】[0011]
【実施例】以下、実施例及び実験例により本発明をさら
に詳しく説明する。 実験1 下記に示した処方において、多価アルコール/水系溶液
中にポリオキシエチレン硬化ヒマシ油を混合させた後、
火成性シリカを混合する方法(製法A)で調製した練歯
磨と、多価アルコール/水系溶液中に火成性シリカを反
応させた後、ポリオキシエチレン硬化ヒマシ油を配合す
る方法(製法B)で調製した練歯磨について、室温にて
1ヵ月経過後の粘度変化および性状変化の評価を行なっ
た。粘度はBH型粘度計で30℃における粘度を測定
し、粘度変化は次の評価基準にしたがって評価した。性
状は肉眼にて次の評価基準にしたがって評価した。結果
を表1に示す。 成 分 配合量(重量%) 火成性シリカ 3.0 沈降性シリカ 13.0 カルボキシメチルセルロースナトリウム 2.0 ソルビット液 表1に示す 水 表1に示す 香料 1.3 サッカリンナトリウム 0.2 ホ゜リオキシエチレン硬化ヒマシ油(60.E.O.) 0.5 合計 100.0% (評価基準) 1.粘度変化 ○:1ヵ月後の粘度/製造直後の粘度の値が、1.0以
上 1.3未満である。 △:1ヵ月後の粘度/製造直後の粘度の値が、1.3以
上 2.0未満である。 ×:1ヵ月後の粘度/製造直後の粘度の値が、2.0以
上である。 2.性状変化 ○:1ヵ月後に分離が認められない。 △:1ヵ月後に若干分離が認められる。 ×:1ヵ月後に分離が認められる。 3.総合評価 ○:粘度、性状とも○である。 △:いずれかに△がある。 ×:いずれかに×がある。EXAMPLES The present invention will be described in more detail with reference to Examples and Experimental Examples. Experiment 1 In the formulation shown below, after mixing polyoxyethylene hydrogenated castor oil in a polyhydric alcohol / water-based solution,
A method of reacting the toothpaste prepared by the method of mixing the igneous silica (manufacturing method A) with the igneous silica in a polyhydric alcohol / water solution, and then blending polyoxyethylene hydrogenated castor oil (manufacturing method B). The toothpaste prepared in () was evaluated for viscosity change and property change after 1 month at room temperature. The viscosity was measured with a BH type viscometer at 30 ° C., and the change in viscosity was evaluated according to the following evaluation criteria. The properties were visually evaluated according to the following evaluation criteria. The results are shown in Table 1. Ingredient content (wt%) Pyrogenic silica 3.0 Precipitable silica 13.0 Sodium carboxymethyl cellulose 2.0 Sorbit liquid Water shown in Table 1 Perfume 1.3 Saccharin sodium 0.2 Polyoxyethylene curing Castor oil (60.EO) 0.5 Total 100.0% (Evaluation criteria) 1. Viscosity change ◯: The value of the viscosity after one month / the viscosity immediately after production is 1.0 or more and less than 1.3. Δ: The value of the viscosity after one month / the viscosity immediately after production is 1.3 or more and less than 2.0. X: The value of the viscosity after one month / the viscosity immediately after production is 2.0 or more. 2. Property change ○: Separation is not observed after 1 month. Δ: Some separation is observed after 1 month. ×: Separation is observed after 1 month. 3. Comprehensive evaluation ◯: Both viscosity and properties are ◯. Δ: There is Δ in either. X: There is x in either.
【0012】[0012]
【表1】 [Table 1]
【0013】実験2 下記の処方において、製法Aに基づき、多価アルコール
/水系溶液中に表2に示した添加剤を混合した後に火成
性シリカを混合し火成性シリカを配合した練歯磨を調整
した。多価アルコールと水の比率は実験1の結果の良好
であった、1:1.8とし、室温にて1ヵ月経過後の粘
度変化および性状変化の評価を行なった。なお、粘度、
粘度変化、性状変化および総合評価は実験1と同じ基準
にしたがって評価した。結果を表2に示す。 成 分 配合量(重量%) 火成性シリカ 3.0 沈降性シリカ 13.0 カルボキシメチルセルロースナトリウム 2.0 香料 1.3 サッカリンナトリウム 0.2 ソルビット液 28.0 水 52.0 添加剤 表2に示す 合計 100.0%Experiment 2 A toothpaste prepared by mixing the additives shown in Table 2 in a polyhydric alcohol / water solution and then mixing the igneous silica with the igneous silica based on the production method A in the following formulation. Was adjusted. The ratio of the polyhydric alcohol and the water was as good as the result of Experiment 1, and was set to 1: 1.8, and the change in viscosity and the change in property after 1 month at room temperature were evaluated. The viscosity,
The change in viscosity, the change in properties and the overall evaluation were evaluated according to the same criteria as in Experiment 1. The results are shown in Table 2. Component content (wt%) Pyrogenic silica 3.0 Precipitable silica 13.0 Sodium carboxymethyl cellulose 2.0 Perfume 1.3 Saccharin sodium 0.2 Sorbit solution 28.0 Water 52.0 Additives Shown in Table 2 Total 100.0%
【0014】[0014]
【表2】 [Table 2]
【0015】[0015]
【発明の効果】本発明によれば、経日で粘度変化の少な
く、保型性の良好な歯磨組成物が得られる。EFFECTS OF THE INVENTION According to the present invention, a dentifrice composition having little change in viscosity over time and good shape retention can be obtained.
Claims (6)
いて、酸化エチレンの付加モル数が40から80である
ポリオキシエチレン硬化ヒマシ油および1:1.4〜
1:2.2の比率の多価アルコール/水を配合したこと
を特徴とする歯磨組成物。Claims: 1. A dentifrice composition containing a fumed silica, wherein polyoxyethylene hydrogenated castor oil in which the added mole number of ethylene oxide is 40 to 80 and 1: 1.4-.
A dentifrice composition comprising a polyhydric alcohol / water in a ratio of 1: 2.2.
アルコール/水系溶液中に混合した後、火成性シリカを
混合することを特徴とする歯磨組成物の製造方法。2. A method for producing a dentifrice composition, which comprises mixing polyoxyethylene hydrogenated castor oil in a polyhydric alcohol / water-based solution and then mixing ignitable silica.
5m2/gである火成性シリカを使用することを特徴と
する請求項1乃至2記載の歯磨組成物およびその製造方
法。3. The specific surface area according to the BET method is 175 to 22.
The dentifrice composition according to claim 1 or 2, and a method for producing the same, which comprises using 5 m 2 / g of ignitable silica.
あり、ポリオキシエチレン硬化ヒマシ油の配合量が0.
1〜2重量%であり、多価アルコールが25〜40重量
%であることを特徴とする請求項1乃至3記載の歯磨組
成物およびその製造方法。4. The blending amount of the igneous silica is 1 to 4% by weight, and the blending amount of the polyoxyethylene hydrogenated castor oil is 0.
The dentifrice composition according to any one of claims 1 to 3 and the method for producing the dentifrice composition, wherein the content is 1 to 2% by weight and the polyhydric alcohol is 25 to 40% by weight.
請求項1乃至4記載の歯磨組成物およびその製造方法。5. The dentifrice composition according to claim 1, wherein a silica-based abrasive is blended as the abrasive, and the method for producing the same.
ズであることを特徴とする請求項1乃至4記載の歯磨組
成物およびその製造方法。6. The dentifrice composition according to claim 1, wherein the dentifrice composition has a viscosity of 350 to 650 poise, and a method for producing the same.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12066394A JPH07304641A (en) | 1994-05-09 | 1994-05-09 | Tooth paste composition and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12066394A JPH07304641A (en) | 1994-05-09 | 1994-05-09 | Tooth paste composition and its production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07304641A true JPH07304641A (en) | 1995-11-21 |
Family
ID=14791827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12066394A Withdrawn JPH07304641A (en) | 1994-05-09 | 1994-05-09 | Tooth paste composition and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07304641A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017223493A1 (en) * | 2016-06-24 | 2017-12-28 | Colgate-Palmolive Company | Oral care compositions and methods of use |
-
1994
- 1994-05-09 JP JP12066394A patent/JPH07304641A/en not_active Withdrawn
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017223493A1 (en) * | 2016-06-24 | 2017-12-28 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| WO2017223497A1 (en) * | 2016-06-24 | 2017-12-28 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| US10588840B2 (en) | 2016-06-24 | 2020-03-17 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| US10617620B2 (en) | 2016-06-24 | 2020-04-14 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| US11207254B2 (en) | 2016-06-24 | 2021-12-28 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| US11234915B2 (en) | 2016-06-24 | 2022-02-01 | Colgate-Palmolive Company | Oral care compositions and methods of use |
| US12329835B2 (en) | 2016-06-24 | 2025-06-17 | Colgate-Palmolive Company | Oral care compositions and methods of use |
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