WO1996001616A1 - Polyglycerol ester composition and method for its production - Google Patents
Polyglycerol ester composition and method for its production Download PDFInfo
- Publication number
- WO1996001616A1 WO1996001616A1 PCT/US1995/009387 US9509387W WO9601616A1 WO 1996001616 A1 WO1996001616 A1 WO 1996001616A1 US 9509387 W US9509387 W US 9509387W WO 9601616 A1 WO9601616 A1 WO 9601616A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- polyglycerol ester
- water
- dentifrice
- polyol
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 91
- 229920000223 polyglycerol Polymers 0.000 title claims abstract description 59
- 150000002148 esters Chemical class 0.000 title claims abstract description 56
- 238000000034 method Methods 0.000 title claims abstract description 13
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 34
- 238000009472 formulation Methods 0.000 claims abstract description 22
- 229920005862 polyol Polymers 0.000 claims abstract description 17
- 150000003077 polyols Chemical class 0.000 claims abstract description 17
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 4
- 239000000194 fatty acid Substances 0.000 claims abstract description 4
- 229930195729 fatty acid Natural products 0.000 claims abstract description 4
- 238000001879 gelation Methods 0.000 claims abstract description 4
- 239000007788 liquid Substances 0.000 claims abstract description 3
- 239000000551 dentifrice Substances 0.000 claims description 32
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 29
- 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 claims description 9
- 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 claims description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000000600 sorbitol Substances 0.000 claims description 9
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 5
- 239000000796 flavoring agent Substances 0.000 claims description 4
- 239000003906 humectant Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 235000013355 food flavoring agent Nutrition 0.000 claims description 3
- 244000005700 microbiome Species 0.000 claims description 3
- WOKDXPHSIQRTJF-UHFFFAOYSA-N 3-[3-[3-[3-[3-[3-[3-[3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)COCC(O)CO WOKDXPHSIQRTJF-UHFFFAOYSA-N 0.000 claims description 2
- 229920001908 Hydrogenated starch hydrolysate Polymers 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- RUSIZKKQGFQEHZ-UHFFFAOYSA-N OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O Chemical group OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O RUSIZKKQGFQEHZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 230000009969 flowable effect Effects 0.000 abstract description 7
- -1 fatty acid ester Chemical class 0.000 abstract description 6
- 239000000047 product Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000006072 paste Substances 0.000 description 5
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 239000000606 toothpaste Substances 0.000 description 4
- 229940034610 toothpaste Drugs 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010418 carrageenan Nutrition 0.000 description 3
- 239000000679 carrageenan Substances 0.000 description 3
- 229920001525 carrageenan Polymers 0.000 description 3
- 229940113118 carrageenan Drugs 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 229940105902 mint extract Drugs 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 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 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 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
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 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
- 238000004090 dissolution Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 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
- 238000003756 stirring Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 230000001225 therapeutic effect Effects 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
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 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 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
- 239000004382 Amylase Substances 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical class C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- 108010001682 Dextranase Proteins 0.000 description 1
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 239000001329 FEMA 3811 Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 101100321817 Human parvovirus B19 (strain HV) 7.5K gene Proteins 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 235000014749 Mentha crispa Nutrition 0.000 description 1
- 244000024873 Mentha crispa Species 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 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
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- PALZHOJEQDADJU-UHFFFAOYSA-N [2-hydroxy-3-[2-hydroxy-3-(2-hydroxy-3-octadecanoyloxypropoxy)propoxy]propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)COCC(O)COC(=O)CCCCCCCCCCCCCCCCC PALZHOJEQDADJU-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940011037 anethole Drugs 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000003212 astringent agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229960003563 calcium carbonate Drugs 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- JUNWLZAGQLJVLR-UHFFFAOYSA-J calcium diphosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229940043256 calcium pyrophosphate Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 235000019821 dicalcium diphosphate Nutrition 0.000 description 1
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
- 229940038472 dicalcium phosphate Drugs 0.000 description 1
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 229940091249 fluoride supplement Drugs 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical class 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
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- ITVGXXMINPYUHD-CUVHLRMHSA-N neohesperidin dihydrochalcone Chemical compound C1=C(O)C(OC)=CC=C1CCC(=O)C(C(=C1)O)=C(O)C=C1O[C@H]1[C@H](O[C@H]2[C@@H]([C@H](O)[C@@H](O)[C@H](C)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 ITVGXXMINPYUHD-CUVHLRMHSA-N 0.000 description 1
- 229940089953 neohesperidin dihydrochalcone Drugs 0.000 description 1
- 235000010434 neohesperidine DC Nutrition 0.000 description 1
- 229960004927 neomycin 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
- 229940049954 penicillin Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 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
- 239000000377 silicon dioxide Substances 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
- 229940079862 sodium lauryl sarcosinate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- AQMNWCRSESPIJM-UHFFFAOYSA-M sodium metaphosphate Chemical compound [Na+].[O-]P(=O)=O AQMNWCRSESPIJM-UHFFFAOYSA-M 0.000 description 1
- 229960004711 sodium monofluorophosphate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- ANOBYBYXJXCGBS-UHFFFAOYSA-L stannous fluoride Chemical compound F[Sn]F ANOBYBYXJXCGBS-UHFFFAOYSA-L 0.000 description 1
- 229960002799 stannous fluoride Drugs 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 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
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2065—Polyhydric alcohols
Definitions
- This invention relates to polyglycerol ester additives for a wide variety of formulations, such as personal care products, particularly dentifrices, containing such additives as surfactants and/or viscosity modifiers.
- Conventional personal care formulations such as dentifrices, generally contain surfactants to increase their cleaning action and provide the foaming properties expected by the user.
- Polyglycerol esters have been used for this purpose, as described in U.S. Patent 4,865,839 to Saso.
- a dentifrice should be formulated to conveniently extrude from a tube as a ribbon, break sharply, and retain integrity for a reasonable period of time on a toothbrush.
- dentifrices containing polyglycerol esters require additional thickeners, such as sodium carboxymethyl cellulose, carrageenan or polyethylene glycol, to control formulation flow properties.
- additional thickeners such as sodium carboxymethyl cellulose, carrageenan or polyethylene glycol
- polyglycerol esters are insoluble in water at room temperature, and the highly viscous solutions which result when the compound is mixed with water cannot readily be added to the dentifrice in a room temperature manufacturing process.
- the polyglycerol esters may be added to the dentifrice formulation using a high temperature processing step, but such a procedure is undesirable because it is not part of the conventional manufacturing processes.
- polyglycerol esters provide many potential benefits in personal care formulations
- the use of these compounds requires incorporation of additional thickening ingredients in the formulation, or a difficult to implement high temperature processing step.
- a polyglycerol ester composition has now been discovered which may be incorporated into personal care products at room temperature in a conventional manufacturing process.
- the resulting personal care products do not require additional thickening agents to control their viscosity.
- the present invention also includes a method of preparing a polyglycerol ester composition for subsequent introduction at room temperature into a personal care formulation.
- the polyglycerol ester is first added to a mixture of a polyol and water at a temperature above room temperature, and allowed to cool to room temperature to produce a polyglycerol ester additive composition.
- the resulting composition is flowable at room temperature, and may easily be incorporated at room temperature into dentifrices and other personal care products.
- the polyglycerol ester composition of the invention makes it possible to prepare personal care products at room temperature which are thickened with polyglycerol esters, and are substantially free of other viscosity modifiers, without altering the conventional manufacturing process.
- the resulting personal care products are an improvement over prior art in that a well performing product can be more simply and economically manufactured with a smaller number of ingredients.
- the polyglycerol ester composition of the invention is formulated with an amount of water sufficient to prevent gelation of the composition at room temperature, i.e., with a viscosity of less than 100K cps, but not so great as to permit the spoilage of the composition by microorganisms such as bacteria, molds and yeasts.
- the properly prepared composition has a long shelf life, i.e., it may be stored for extended periods, e.g., up to six months.
- the polyglycerol ester composition of the invention may be utilized as a surfactant and viscosity modifier in a wide variety of formulations. It is provided as a liquid composition which, while flowable at room temperature, thickens to the desired viscosity upon the introduction of additional formulation ingredients.
- the polyglycerol ester composition of the invention comprises about 1 to 5 wt% of a polyglycerol fatty acid ester, about 1 to 20 wt% of water, and about 75 to 95 wt% of a polyol. It generates the desired viscosity when incorporated into a personal care formulation.
- the polyglycerol esters have 6 to 12 glycerol units, more preferably, 6 to 10, 1 to 3 ester linkages, more preferably, 1 or 2.
- the fatty acids used for esterification may have from 10 to 20 carbon atoms, preferably, from 12 to 18.
- polyglycerol esters are hexaglyceryl distearate, decaglyceryl mono- and dipalmitate, decaglyceryl mono and distearate, and mixtures thereof.
- the preferred polyglycerol esters are decaglyceryl distearate and decaglyceryl dipalmitate.
- the polyols which can be utilized in the composition of the invention may vary widely and include any polyol which is compatible with the polyglycerol ester and the resultant personal care formulation.
- Typical examples of polyols which may be used include glycerol, polyglycerol, propylene glycol, sorbitol and hydrogenated starch hydrolysates.
- the preferred polyols are glycerol and sorbitol, and the most preferred is glycerol.
- Mixtures of polyols may also be used, such as, mixtures of sorbitol and glycerol or mixtures of sorbitol with polyglycerols.
- the water utilized in formulating the composition of the invention should be of a high purity, e.g., deionized water or distilled water.
- the amount added is such that the water activity of the finished solution is below 0.7 and preferably below 0.5.
- the water activity is the relative humidity over the solution at a given temperature, and is measured with a hygrometer, such as the AquaLab, manufactured by Decagon Devices, Pullman, Washington. If the water activity level is maintained below 0.7, no preservatives need be added to the composition of the invention and a long shelf life is assured.
- the composition of the invention is prepared by dissolving the polyglycerol ester in a solution containing the polyol and water.
- the dissolution is performed at a temperature of about 60 °C to about 80 °C with stirring, preferably, at about 75 °C.
- the composition is cooled to room temperature.
- the amount of water added to the composition of the invention should be sufficient to prevent gelation of the composition at temperatures from about 15 to 30°C.
- the amount needed varies depending on the particular polyglycerol ester employed.
- the viscosity of the solution should not be above about 150K cps at a temperature of 25 °C, as measured by a Brookfield Viscometer. Typical viscosities range from about 5K cps to 100K cps, preferably, about 10K cps to 40K cps, at a temperature of 25 °C.
- composition of the invention may be prepared well in advance at a different location from the final product, as for example by the supplier of the polyglycerol esters.
- the shelf life is normally in excess of about 6 months.
- the polyglycerol ester composition may be utilized alone to control the texture and flow properties of a personal care formulations, or in combination with a minor amount of other conventional viscosity modifiers such as, for example, sodium carboxymethyl cellulose, carrageenan or polyethylene glycol.
- the effective amount is about 0.5% by weight to about 2 wt%, preferably, about 1 wt%. These ranges are particularly applicable to a dentifrice.
- the dentifrices may include a wide variety of conventional ingredients which are well known in the art.
- abrasives such as silicas, calcium carbonate, dicalcium phosphate, calcium pyrophosphate, insoluble sodium metaphosphate, and silicic anhydride
- humectants such as glycerol, sorbitol, hydrogenated starch hydroiysates, propylene glycol and polyethylene glycol
- binders such as carboxymethyl cellulose, carrageenan, sodium alginate, locust bean gum, hydroxyethyl cellulose and polyvinyl alcohol
- sweeteners such as sodium saccharin, glycyrrhizin salts, steviocide, neohesperidin dihydrochalcone, p-methoxycinnamic aldehyde and perillartine
- flavors such as carvone, anethole, peppermint, spearmint and cinnamon
- bactericides such as fluor
- a typical dentifrice formulation which may be made using the composition of the invention is composed of 30 to 70 wt% of a polyol humectant, such as USP sorbitol; 10 to 50 wt% of an abrasive, such as Zeodent ® 1 13 or 165 (Zeodent is a trademark for precipitated silica abrasives made by the J.M. Huber Corp.); 0.3 to 2 wt% of the polyglycerol ester; and further includes a small amount of a flavoring agent, such as mint extract.
- the composition generally contains about 5 to 30 wt% water. To more fully illustrate the invention the following examples are presented. It will be understood, however, that these examples are not intended to limit the scope of the invention.
- the polyglycerol ester composition and the dentifrice formulation were easily mixed by hand with a spatula until a smooth paste was formed.
- the resulting paste could be easily extruded from a tube and retained its integrity for a reasonable time when applied to a toothbrush.
- the paste showed no syneresis after six month storage at 25 °C, illustrating that dentifrices prepared with the polyglycerol ester composition of the invention will maintain their viscosity over an extended period.
- Viscosity 25 °C
- compositions were prepared to establish the most useful range of ingredients compatible with the conventional dentifrice manufacturing process, while still producing a toothpaste with good shelf-stability.
- Part B A therapeutic solution for forming a dentifrice was prepared by mixing of 195 parts by weight of 70% USP sorbitol, 1.2 parts by weight sodium fluoride, and 8 parts by weight water. To produce the dentifrice, 29.4 g of the polyglycerol ester Composition C were admixed and blended at room temperature with 40.8 g of the therapeutic solution, 18.0 g Zeodent 113, 5.5 g Zeodent 165, and 0.5 ml mint extract. The blending was easily done by hand at room temperature with a spatula.
- Composition A which contained 3.5 parts of the polyglycerol ester and 14.5 parts of water, formed a non-flowable gel when cooled to room temperature, and could not be blended with a dentifrice formulation.
- Composition B in which the amount of polyglycerol ester was reduced to 1.7 parts, was less viscous than composition A, but was too viscous at room temperature to easily blend with a dentifrice formulation.
- Composition C in which the amount of polyglycerol ester was reduced to 1 part by weight, contained a sufficient amount of water, about 15 parts, to flow easily at room temperature and blend with the dentifrice formulation to form a toothpaste.
- Composition C also contained sufficient amounts of polyglycerol ester such that, when the dentifrice was added, the composition thickened and formed a toothpaste which could be conveniently extruded from a tube, and which retained its integrity for a reasonable period of time on a toothbrush.
- the dentifrice paste produced using composition C did not develop any syneresis following storage at room temperature for 6 months; the paste made with composition D failed after one week.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
Abstract
A flowable liquid composition comprising about 1 to 5 wt.% of a polyglycerol fatty acid ester, about 1 to 20 wt.% by weight of water and about 75 to 95 wt.% of a polyol; a method for producing such compositions; and personal care formulations contain such compositions. The method includes dissolving a polyglycerol ester at a temperature from about 60 °C to 80 °C in solution comprising a polyol and water, the amount of water being sufficient to prevent gelation of the composition at room temperature.
Description
POLYGLYCEROL ESTER COMPOSITION AND METHOD FOR ITS PRODUCTION
BACKGROUND OF THE INVENTION
This invention relates to polyglycerol ester additives for a wide variety of formulations, such as personal care products, particularly dentifrices, containing such additives as surfactants and/or viscosity modifiers.
Conventional personal care formulations, such as dentifrices, generally contain surfactants to increase their cleaning action and provide the foaming properties expected by the user. Polyglycerol esters have been used for this purpose, as described in U.S. Patent 4,865,839 to Saso.
A dentifrice should be formulated to conveniently extrude from a tube as a ribbon, break sharply, and retain integrity for a reasonable period of time on a toothbrush. To provide the proper texture, dentifrices containing polyglycerol esters require additional thickeners, such as sodium carboxymethyl cellulose, carrageenan or polyethylene glycol, to control formulation flow properties. (See, for example, Jpn. Kokai JP 62 45,513 (1987)). In recent years, the toxicity and environmental effects of some of these compounds, particularly the ethoxylated compounds commonly used as thickeners, have been questioned. If high levels of polyglycerol esters could be incorporated into the dentifrice, it would be possible to limit or eliminate the need for the potentially harmful thickening agents. However, polyglycerol esters are insoluble in water at room temperature, and the highly viscous solutions
which result when the compound is mixed with water cannot readily be added to the dentifrice in a room temperature manufacturing process. The polyglycerol esters may be added to the dentifrice formulation using a high temperature processing step, but such a procedure is undesirable because it is not part of the conventional manufacturing processes.
Thus, while polyglycerol esters provide many potential benefits in personal care formulations, the use of these compounds requires incorporation of additional thickening ingredients in the formulation, or a difficult to implement high temperature processing step.
SUMMARY OF THE INVENTION
In accordance with the invention, a polyglycerol ester composition has now been discovered which may be incorporated into personal care products at room temperature in a conventional manufacturing process. The resulting personal care products do not require additional thickening agents to control their viscosity.
The present invention also includes a method of preparing a polyglycerol ester composition for subsequent introduction at room temperature into a personal care formulation. In the method of the invention, the polyglycerol ester is first added to a mixture of a polyol and water at a temperature above room temperature, and allowed to cool to room temperature to produce a polyglycerol ester additive composition. The resulting composition is flowable at room temperature, and may easily be incorporated at room temperature into dentifrices and other personal care products.
The polyglycerol ester composition of the invention makes it possible to prepare personal care products at room temperature which are thickened with polyglycerol esters, and are substantially free of other viscosity modifiers, without altering the conventional manufacturing process. The resulting personal care products are an improvement over prior art in that a well performing product can be more simply and economically manufactured with a smaller number of ingredients.
The polyglycerol ester composition of the invention is formulated with an amount of water sufficient to prevent gelation of the composition at room temperature, i.e., with a viscosity of less than 100K cps, but not so great as to permit the spoilage of the composition by microorganisms such as bacteria, molds and yeasts. Thus, the properly prepared composition has a long shelf life, i.e., it may be stored for extended periods, e.g., up to six months.
DETAILED DESCRIPTION OF THE INVENTION The polyglycerol ester composition of the invention may be utilized as a surfactant and viscosity modifier in a wide variety of formulations. It is provided as a liquid composition which, while flowable at room temperature, thickens to the desired viscosity upon the introduction of additional formulation ingredients. Broadly, the polyglycerol ester composition of the invention comprises about 1 to 5 wt% of a polyglycerol fatty acid ester, about 1 to 20 wt% of water, and about 75 to 95 wt% of a polyol. It generates the desired viscosity when incorporated into a personal care formulation.
Broadly, the polyglycerol esters have 6 to 12 glycerol units, more preferably, 6 to 10, 1 to 3 ester linkages, more preferably, 1 or 2. The fatty acids used for esterification may have from 10 to 20 carbon atoms, preferably, from 12 to 18.
Typical examples of polyglycerol esters are hexaglyceryl distearate, decaglyceryl mono- and dipalmitate, decaglyceryl mono and distearate, and mixtures thereof. The preferred polyglycerol esters are decaglyceryl distearate and decaglyceryl dipalmitate.
The polyols which can be utilized in the composition of the invention may vary widely and include any polyol which is compatible with the polyglycerol ester and the resultant personal care formulation. Typical examples of polyols which may be used include glycerol, polyglycerol, propylene glycol, sorbitol and hydrogenated starch hydrolysates. The preferred polyols are glycerol and sorbitol, and the most preferred is glycerol.
Mixtures of polyols may also be used, such as, mixtures of sorbitol and glycerol or mixtures of sorbitol with polyglycerols.
The water utilized in formulating the composition of the invention should be of a high purity, e.g., deionized water or distilled water. The amount added is such that the water activity of the finished solution is below 0.7 and preferably below 0.5. The water activity is the relative humidity over the solution at a given temperature, and is measured with a hygrometer, such as the AquaLab, manufactured by Decagon Devices, Pullman, Washington. If the water activity level is maintained below 0.7, no preservatives need be added to the composition of the invention and a long shelf life is assured.
The composition of the invention is prepared by dissolving the polyglycerol ester in a solution containing the polyol and water. The dissolution is performed at a temperature of about 60 °C to about 80 °C with stirring, preferably, at about 75 °C. Following dissolution, the composition is cooled to room temperature.
The amount of water added to the composition of the invention should be sufficient to prevent gelation of the composition at temperatures from about 15 to 30°C. The amount needed varies depending on the particular polyglycerol ester employed. The viscosity of the solution should not be above about 150K cps at a temperature of 25 °C, as measured by a Brookfield Viscometer. Typical viscosities range from about 5K cps to 100K cps, preferably, about 10K cps to 40K cps, at a temperature of 25 °C.
Because of its long shelf-life, the composition of the invention may be prepared well in advance at a different location from the final product, as for example by the supplier of the polyglycerol esters. The shelf life is normally in excess of about 6 months.
The polyglycerol ester composition may be utilized alone to control the texture and flow properties of a personal care formulations, or in combination with a minor amount of other conventional viscosity modifiers such as, for example, sodium carboxymethyl cellulose, carrageenan or polyethylene glycol. Typically, the effective amount is about 0.5% by weight
to about 2 wt%, preferably, about 1 wt%. These ranges are particularly applicable to a dentifrice.
The dentifrices may include a wide variety of conventional ingredients which are well known in the art. For example, abrasives such as silicas, calcium carbonate, dicalcium phosphate, calcium pyrophosphate, insoluble sodium metaphosphate, and silicic anhydride; humectants such as glycerol, sorbitol, hydrogenated starch hydroiysates, propylene glycol and polyethylene glycol; binders such as carboxymethyl cellulose, carrageenan, sodium alginate, locust bean gum, hydroxyethyl cellulose and polyvinyl alcohol; sweeteners such as sodium saccharin, glycyrrhizin salts, steviocide, neohesperidin dihydrochalcone, p-methoxycinnamic aldehyde and perillartine; flavors such as carvone, anethole, peppermint, spearmint and cinnamon; bactericides such as fluorides and chlorohexidine salts; phosphate compounds such as sodium phosphate; enzymes such as dextranase and amylase; anti- inflammatory compounds such as E-aminocaproic acid, tranexamic acid and allantoinate; anti-tartar agents; preservatives, such as benzoate and benzoic acid derivatives; colorants, such as FD&C dyes, D&C dyes and pigments; surfactants, such as sodium lauryl sulfate, sodium lauryl sarcosinate and others listed in Accepted Dental Therapeutics; buffers, such as phosphates, acetates and citrates; astringents, such as zinc chloride and aluminum salts; antibiotics, such as penicillin neomycin; fluoride compounds, such as sodium fluoride, sodium monofluorophosphate, stannous fluoride and organic fluoride; and, other effective compounds.
A typical dentifrice formulation which may be made using the composition of the invention is composed of 30 to 70 wt% of a polyol humectant, such as USP sorbitol; 10 to 50 wt% of an abrasive, such as Zeodent® 1 13 or 165 (Zeodent is a trademark for precipitated silica abrasives made by the J.M. Huber Corp.); 0.3 to 2 wt% of the polyglycerol ester; and further includes a small amount of a flavoring agent, such as mint extract. The composition generally contains about 5 to 30 wt% water.
To more fully illustrate the invention the following examples are presented. It will be understood, however, that these examples are not intended to limit the scope of the invention.
EXAMPLE 1
3.5 parts by weight of decaglyceryl distearate were dissolved with stirring in a solution of 82 parts by weight of glycerol and 14.5 parts by weight distilled water at 75 °C. Upon cooling to room temperature the solution remained flowable. A similarly prepared solution without the added water formed a non-flowable gel when cooled to room temperature. 30.5 g of the above polyglycerol ester composition were admixed and blended at room temperature with a dentifrice formulation consisting of 39.3 g of 70% USP sorbitol, 1.7 g water, 0.5 ml of mint extract, as well as 18.0 g Zeodent 113 and 5.5 g Zeodent 165. The polyglycerol ester composition and the dentifrice formulation were easily mixed by hand with a spatula until a smooth paste was formed. The resulting paste could be easily extruded from a tube and retained its integrity for a reasonable time when applied to a toothbrush.
The paste showed no syneresis after six month storage at 25 °C, illustrating that dentifrices prepared with the polyglycerol ester composition of the invention will maintain their viscosity over an extended period.
EXAMPLE 2 Part A The following polyglycerol ester compositions, in parts by weight, were prepared by blending the components at 75 °C:
A B C D
Glycerol 82 82 85 85
Decaglycerol Dipalmitate 3.5 1.7 1 0.8
Water 14.5 14.5 15 15
A B C D
Viscosity (25 °C), Centipoise 320K 64K 14K 7.5K
Flowability (25 °C) gels vise flows flows
The above compositions were prepared to establish the most useful range of ingredients compatible with the conventional dentifrice manufacturing process, while still producing a toothpaste with good shelf-stability.
Part B A therapeutic solution for forming a dentifrice was prepared by mixing of 195 parts by weight of 70% USP sorbitol, 1.2 parts by weight sodium fluoride, and 8 parts by weight water. To produce the dentifrice, 29.4 g of the polyglycerol ester Composition C were admixed and blended at room temperature with 40.8 g of the therapeutic solution, 18.0 g Zeodent 113, 5.5 g Zeodent 165, and 0.5 ml mint extract. The blending was easily done by hand at room temperature with a spatula.
Composition A, which contained 3.5 parts of the polyglycerol ester and 14.5 parts of water, formed a non-flowable gel when cooled to room temperature, and could not be blended with a dentifrice formulation. Composition B, in which the amount of polyglycerol ester was reduced to 1.7 parts, was less viscous than composition A, but was too viscous at room temperature to easily blend with a dentifrice formulation. Composition C; in which the amount of polyglycerol ester was reduced to 1 part by weight, contained a sufficient amount of water, about 15 parts, to flow easily at room temperature and blend with the dentifrice formulation to form a toothpaste. Composition C also contained sufficient amounts of polyglycerol ester such that, when the dentifrice was added, the composition thickened and formed a toothpaste which could be conveniently extruded from a tube, and which retained its integrity for a reasonable period of time on a toothbrush. A control formula without any polyglycerol ester, while flowable at room temperature and easily blended with the dentifrice formulation, did not develop sufficient viscosity following addition of the dentifrice ingredients to form a toothpaste with acceptable texture.
The dentifrice paste produced using composition C did not develop any syneresis following storage at room temperature for 6 months; the paste made with composition D failed after one week.
Claims
What is claimed is: 1. A composition which comprises about 1 to 5 wt% of a polyglycerol ester, about 1 to 20 wt% water, and about 75 to about 95 wt% of a polyol, said composition having a viscosity of less than 150K cps at 25°C.
2. The composition of claim 1 , wherein the polyol is selected from the group consisting of glycerol, polyglycerols, sorbitol, propylene glycol, hydrogenated starch hydrolysates and mixtures thereof.
3. The composition of claim 1 , wherein the polyglycerol ester has from 6 to 12 glycerol units and from 1 to 3 ester groups.
4. The composition of claim 3, wherein the fatty acids portion of the ester has from 10 to 20 carbon atoms.
5. The composition of claim 1 , wherein the polyglycerol ester is hexaglycerol distearate, decaglyceryl monopalmitate, decaglyceryl dipalmitate, decaglycerol monostearate, decaglyceryl distearate, or mixtures thereof.
6. The composition of claim 1 , wherein said composition has a water activity of about 0.5 to about 0.7.
7. The composition of claim 1 , wherein the water present does not sustain the growth of microorganisms.
8. A method for producing a polyglycerol ester composition which comprises: dissolving a polyglycerol ester in a solution of a polyol and water at a temperature of about 60 °C to 80 °C; the amount of water being sufficient to prevent gelation of said composition at room temperature, so as to form a homogeneous liquid having a viscosity of less than 100K cps at 25 °C.
9. The method of claim 8, wherein said composition has a water activity of about 0.5 to 0.7.
10. The method of claim 8, wherein the water in the solution is not sufficient to sustain the growth of microorganisms.
1 1. A method for producing a polyglycerol ester composition which comprises dissolving at a temperature of about 60 °C to 80 °C, about 1 to 5 wt% of a polyglycerol ester in a solution comprising about 75 to 95 wt% of a polyol and about 1 to about 20 wt% of water.
12. A process for producing a dentifrice comprising: (a) formulating a polyglycerol ester composition by dissolving at a temperature from about 60 °C to 80 °C, about 1 to 5 wt% of a polyglycerol ester in a solution of about 75 to 95 wt% of a polyol and at least 1 wt% of water; (b) cooling the polyglycerol ester composition to room temperature; (c) blending at room temperature from about 25 to 40 wt% of said polyglycerol ester composition, based on the total weight of the dentifrice, with a formulation comprising a humectant, an abrasive and a flavoring agent.
13. The process of claim 12, wherein said formulation also contains a therapeutic agent.
14. The process of claim 12, wherein said dentifrice is substantially free of viscosity modifiers other than the polyglycerol ester.
15. The process of claim 12 wherein the polyglycerol ester composition has a viscosity less than 100K cps at 25 °C.
16. The process of claim 12, wherein said polyglycerol ester is decaglyceryl dipalmitate or decaglyceryl distearate, and said polyol is glycerol
17. A dentifrice comprising from about 10 to 50 wt% of an abrasive; about 0.3 to 2 wt% of a polyglycerol ester; 30 to 70% of a humectant and about 5 to 30 wt% water.
18. The dentifrice of claim 17, further comprising a flavoring agent.
19. The dentifrice of claim 18, further comprising a therapeutic agent.
20. The dentifrice of claim 17, wherein said dentifrice is substantially free of viscosity modifiers other than the polyglycerol ester.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU31461/95A AU3146195A (en) | 1994-07-11 | 1995-07-10 | Polyglycerol ester composition and method for its production |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27340394A | 1994-07-11 | 1994-07-11 | |
US273,403 | 1994-07-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996001616A1 true WO1996001616A1 (en) | 1996-01-25 |
Family
ID=23043796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/009387 WO1996001616A1 (en) | 1994-07-11 | 1995-07-10 | Polyglycerol ester composition and method for its production |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU3146195A (en) |
IL (1) | IL114550A0 (en) |
WO (1) | WO1996001616A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8466100B2 (en) | 2008-08-15 | 2013-06-18 | The Procter & Gamble Company | Benefit compositions comprising polyglycerol esters |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4435380A (en) * | 1982-01-29 | 1984-03-06 | Lever Brothers Company | Humectants for clear gel dentifrice compositions |
US4865839A (en) * | 1986-09-02 | 1989-09-12 | Lion Corporation | Oral composition containing a polyglycerol fatty acid monoester and an N-acylamino acid or a salt thereof |
US5109127A (en) * | 1989-11-06 | 1992-04-28 | Lion Corporation | Nonionic surface active agent |
US5130060A (en) * | 1983-10-14 | 1992-07-14 | Igor Beseda | Method of manufacturing polyglycerol esters |
US5154855A (en) * | 1989-11-14 | 1992-10-13 | Lion Corporation | Emulsified composition |
-
1995
- 1995-07-10 WO PCT/US1995/009387 patent/WO1996001616A1/en active Application Filing
- 1995-07-10 AU AU31461/95A patent/AU3146195A/en not_active Abandoned
- 1995-07-11 IL IL11455095A patent/IL114550A0/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4435380A (en) * | 1982-01-29 | 1984-03-06 | Lever Brothers Company | Humectants for clear gel dentifrice compositions |
US5130060A (en) * | 1983-10-14 | 1992-07-14 | Igor Beseda | Method of manufacturing polyglycerol esters |
US4865839A (en) * | 1986-09-02 | 1989-09-12 | Lion Corporation | Oral composition containing a polyglycerol fatty acid monoester and an N-acylamino acid or a salt thereof |
US5109127A (en) * | 1989-11-06 | 1992-04-28 | Lion Corporation | Nonionic surface active agent |
US5154855A (en) * | 1989-11-14 | 1992-10-13 | Lion Corporation | Emulsified composition |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8466100B2 (en) | 2008-08-15 | 2013-06-18 | The Procter & Gamble Company | Benefit compositions comprising polyglycerol esters |
Also Published As
Publication number | Publication date |
---|---|
IL114550A0 (en) | 1995-11-27 |
AU3146195A (en) | 1996-02-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0177303B1 (en) | Bactericidal toothpastes | |
EP2585031B1 (en) | Non-aqueous oral care compositions | |
US5716600A (en) | Stable stannous fluoride toothpaste compositions | |
US3887701A (en) | Antibacterial oral compositions containing preservative-antioxidants | |
EP0331617A1 (en) | Non-bleeding striped dentifrice | |
JPS6234013B2 (en) | ||
US3842168A (en) | Method of preparing stable dentifrice | |
US4309409A (en) | Anti-corrosion formulation for toothpastes | |
CA1147265A (en) | Toothpaste | |
US7049299B2 (en) | Method for preparing toothpaste using a specific sorbitol syrup, and sorbitol syrup | |
CA1146868A (en) | Sorbitol and polyvinyl pyrrolidone in toothpaste | |
US4877602A (en) | Transparent dentifrices | |
US4264579A (en) | Dentifrices | |
JPS6221327B2 (en) | ||
JPH0725658B2 (en) | Oral composition | |
NZ200379A (en) | Dentifrice composition | |
US4426373A (en) | Smooth dental cream | |
WO1996001616A1 (en) | Polyglycerol ester composition and method for its production | |
JPS6320408B2 (en) | ||
JPS6075412A (en) | Dentifrice composition | |
JPS6215523B2 (en) | ||
JPH0676306B2 (en) | Oral composition | |
JP3482323B2 (en) | Oral composition | |
JPS58118506A (en) | Composition for oral cavity | |
JPS6221763B2 (en) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AM AT AU BB BG BR BY CA CH CN CZ DE DK EE ES FI GB GE HU IS JP KE KG KP KR KZ LK LR LT LU LV MD MG MN MX NO NZ PL PT RO RU SD SE SG SI SK TJ TM TT UA US UZ VN |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): KE MW SD SZ UG AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
122 | Ep: pct application non-entry in european phase | ||
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
NENP | Non-entry into the national phase |
Ref country code: CA |