EP0764013A1 - Denture stabilizing compositions - Google Patents
Denture stabilizing compositionsInfo
- Publication number
- EP0764013A1 EP0764013A1 EP95923006A EP95923006A EP0764013A1 EP 0764013 A1 EP0764013 A1 EP 0764013A1 EP 95923006 A EP95923006 A EP 95923006A EP 95923006 A EP95923006 A EP 95923006A EP 0764013 A1 EP0764013 A1 EP 0764013A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition according
- copolymer
- mixtures
- polyethylene glycol
- average molecular
- 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- Withdrawn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 60
- 230000000087 stabilizing effect Effects 0.000 title description 10
- 229920001577 copolymer Polymers 0.000 claims abstract description 39
- 150000003839 salts Chemical class 0.000 claims abstract description 38
- 239000000853 adhesive Substances 0.000 claims abstract description 30
- 230000001070 adhesive effect Effects 0.000 claims abstract description 24
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 21
- 239000002202 Polyethylene glycol Substances 0.000 claims abstract description 17
- 229910052725 zinc Inorganic materials 0.000 claims description 18
- 239000011701 zinc Substances 0.000 claims description 18
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 17
- -1 strontium cations Chemical class 0.000 claims description 17
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 16
- 239000011575 calcium Substances 0.000 claims description 14
- 229910052791 calcium Inorganic materials 0.000 claims description 14
- 125000002091 cationic group Chemical group 0.000 claims description 14
- 229910052712 strontium Inorganic materials 0.000 claims description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 10
- 239000011734 sodium Substances 0.000 claims description 8
- 229910052708 sodium Inorganic materials 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 7
- 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 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 5
- 239000003086 colorant Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000003755 preservative agent Substances 0.000 claims description 4
- 229920001059 synthetic polymer Polymers 0.000 claims description 4
- 239000002562 thickening agent Substances 0.000 claims description 4
- 150000001719 carbohydrate derivatives Chemical class 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920001206 natural gum Polymers 0.000 claims description 3
- 239000003981 vehicle Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 description 10
- 150000008064 anhydrides Chemical group 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 6
- 239000004264 Petrolatum Substances 0.000 description 5
- 239000001768 carboxy methyl cellulose Substances 0.000 description 5
- 210000000214 mouth Anatomy 0.000 description 5
- 235000019271 petrolatum Nutrition 0.000 description 5
- 229940066842 petrolatum Drugs 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 4
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 229940042472 mineral oil Drugs 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004353 Polyethylene glycol 8000 Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 2
- 229940085678 polyethylene glycol 8000 Drugs 0.000 description 2
- 235000019446 polyethylene glycol 8000 Nutrition 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- 159000000008 strontium salts Chemical class 0.000 description 2
- 229960000834 vinyl ether Drugs 0.000 description 2
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 2
- 229940007718 zinc hydroxide Drugs 0.000 description 2
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 2
- 239000011787 zinc oxide Substances 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
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-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
- LPEKGGXMPWTOCB-UHFFFAOYSA-N 8beta-(2,3-epoxy-2-methylbutyryloxy)-14-acetoxytithifolin Natural products COC(=O)C(C)O LPEKGGXMPWTOCB-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- VUNOFAIHSALQQH-UHFFFAOYSA-N Ethyl menthane carboxamide Chemical compound CCNC(=O)C1CC(C)CCC1C(C)C VUNOFAIHSALQQH-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- SOWBFZRMHSNYGE-UHFFFAOYSA-N Monoamide-Oxalic acid Natural products NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 241000934878 Sterculia Species 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000008122 artificial sweetener Substances 0.000 description 1
- 239000000227 bioadhesive Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- ODQWQRRAPPTVAG-GZTJUZNOSA-N doxepin Chemical compound C1OC2=CC=CC=C2C(=C/CCN(C)C)/C2=CC=CC=C21 ODQWQRRAPPTVAG-GZTJUZNOSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229940014259 gelatin Drugs 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
- 239000000231 karaya gum Substances 0.000 description 1
- 229940039371 karaya gum Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229940057867 methyl lactate Drugs 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 238000002103 osmometry Methods 0.000 description 1
- 229930004008 p-menthane Natural products 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000001953 sensory effect Effects 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
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 150000003438 strontium compounds Chemical class 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/30—Compositions for temporarily or permanently fixing teeth or palates, e.g. primers for dental adhesives
- A61K6/35—Preparations for stabilising dentures in the mouth
Definitions
- Denture stabilizers are used to fill the interstices between the dentures and the gums or tissues. Prior to placement of the denture in the oral cavity, a denture stabilizer is applied to the denture-plate surface which, for a perfect fit, should uniformly contact the gums and mucous tissues.
- the denture stabilizer is formulated not only for its adherent properties, but also to provide a cushion or gasket between the denture and the gums or tissues, thereby positioning the denture securely in the oral cavity.
- a denture stabilizer can be formulated having excellent adhesive quality while ooang less and providing pleasing aesthetics to the user.
- the invention adhesive compositions may also be effectively used as a wound dressing, underwater adhesive, bio-adhesive, and/or as a delivery vehicle for other actives. It is an object of the present invention to provide a hydrophilic denture stabilizing composition which effectively holds dentures in place for prolonged periods of time yet allows for easy removal of the denture on demand. It is also an object of the invention to provide an improved denture stabilizing composition which oozes less than currently available stabilizers and is aesthetically pleasing to the user. It is a further object that the hydrophilic nature of the invention compositions will provide adhesive compositions that are easier to clean from the mouth and/or denture than currently available products.
- the present invention encompasses adhesive compositions comprising: a) from about 10% to about 80% of a mixed partial salt of a lower alkyl vinyl ether- maleic acid copolymer consisting essentially of the repeated structural unit:
- R represents a Cl to C4 alkyl radical
- n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 2SC, and wherein the partial salt contains a cationic salt function of from about 0.1% to about 65% zinc or strontium cations or mixtures thereof, of the total initial carboxyl groups reacted; and b) from about 20% to about 90% of polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600.
- the adhesive compositions of the present invention comprise the mixed partial salt of a lower alkyl vinyl ether-maleic acid copolymer consisting of zinc and/or strontium salts, and polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600. Polyethylene glycol having an average molecular weight of about 400 is most preferred for use in the present invention compositions.
- the present compositions may be formulated as creams, pastes, powders, liquids, ointments, and lotions. A detailed description of essential and optional components of the present invention is given below. Lower Alkyl Vinyl Ether-Maleic Acid Copolymer Salts
- the present adhesive compositions comprise the mixed partial salt of a lower alkyl vinyl ether-maleic acid ("AVE/MA”) copolymer consisting essentially of the repeated structural unit:
- R represents a Cl to C4 alkyl radical
- n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 25C
- the partial salts contain a cationic salt function of from about 0.1% to about 65% zinc and/or strontium cations, preferably from about 10% to about 45%, and most preferably from about 15% to about 30%, of the total initial carboxyl groups reacted.
- mixed partial salt refers to «zinc and/or strontium partial salts of lower alkyl vinyl ether-maleic acid copolymers where the zinc and strontium are mixed on the same copolymer with each other or with other ester functions or nonidentical cations selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof.
- Preferred are mixed partial copolymer salts containing zinc and calcium cations.
- the cationic salt function preferably further consists of from about 0.1% to about 75% metal salts selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof.
- additional metal salts are calcium or sodium metal salts or mixtures thereof.
- Calcium cations may be present at a level of from about 10% to about 75%, preferably from about 25% to about 60%, and most preferably from about 40% to about 60%, of the total initial carboxyl groups reacted.
- Sodium cations may be present at a level of from about 1% to about 20%, preferably from about 1% to about 15%, and most preferably from about 1% to about 10%, of the total initial carboxyl groups reacted.
- the subject polymeric salts are advantageously prepared by the interaction of the AVE/MA copolymer (I) with cationic zinc and/or strontium compounds and preferably at least one calcium, sodium, magnesium, potassium, or ammonium compound having a functional group typical of reactants of a carboxylic acid, such as, for example, the hydroxide, acetate, halide, lactate, etc. in an aqueous medium.
- a carboxylic acid such as, for example, the hydroxide, acetate, halide, lactate, etc.
- the oxide of anc .and the hydroxide of calcium are utilized. Since zinc hydroxide is not commercially available, its use as a reactant is readily and more economically accomplished by employing an aqueous slurry of particular zinc oxide which, although practically insoluble in water, provides hydration to zinc hydroxide on the paniculate surface.
- Strontium hydroxide on the other hand, is available in either crystalline or powder form and is soluble in about 50 parts water. Aqueous solutions of strontium oxide, however, which forms the hydroxide when treated with water (caution: heat evolution), may also be used.
- Anions that form toxic, irritating or contaminating by-products should be avoided, or special precautions and treatment provided to assure the removal and absence of such by-products from the polymeric salt end-product.
- the particular compound used should be substantially pure to assure obtaining a substantially pure, substantially off-white polymeric .salt end-product.
- the lower alkyl vinyl ether maleic acid (AVE/MA) copolymers are readily obtained by copolymerizing a lower alkyl vinyl ether monomer, such as methyl vinyl ether, ethyl vinyl ether, divinyl ether, propyl vinyl ether and isobutyl vinyl ether, with maleic anhydride to yield the corresponding lower alkyl vinyl ether-maleic anhydride copolymer which is readily hydrolyzable to the acid copolymer (I).
- a lower alkyl vinyl ether monomer such as methyl vinyl ether, ethyl vinyl ether, divinyl ether, propyl vinyl ether and isobutyl vinyl ether
- maleic anhydride to yield the corresponding lower alkyl vinyl ether-maleic anhydride copolymer which is readily hydrolyzable to the acid copolymer (I).
- Both anhydride and acid forms are also available from commercial suppliers. For example, the GAF Corporation, Wayne, N.J.
- GANTREZ S-97 M. W. TM 50,000
- the acid and anhydride forms of AVE/MA copolymers having an average molecular weight of from about 50,000 to about 80,000 (as measured by membrane osmometry in 2-butanone 1-10 grams/ 1000 ml solution), are also characterized by having the previously described specific viscosity parameter of more than 1.2.
- the anhydride copolymer dissolves in water, the anhydride linkage is cleaved so that the highly polar, polymeric free acid (I) is formed.
- the anhydride form which is relatively less expensive than the acid form, may be used as a convenient and cheaper precursor for the acid. Elevated temperatures may be advantageously employed to enhance the rate of anhydride-to-acid hydrolysis.
- the lower alkyl vinyl ether-maleic acid copolymer (I), or its corresponding anhydride is added to water preheated to about 70°-80°C. with vigorous stirring to form a homogeneous mixture. If the anhydride precursor is utilized, it is recommended that the aqueous mixture be further heated to about 90° C. with stirring to ensure complete hydrolysis of the anhydride to the acid form. Heating is then discontinued although mixing is continued until the batch turns clear with a simultaneous decrease in viscosity (about 65°-75°C.).
- An aqueous solution of the cationic zinc and/or strontium salt forming compound, or, for example, an aqueous dispersion of paniculate zinc oxide is combined with calcium hydroxide in the form of a slurry, in an amount sufficient to provide the desire cationic content desired in the end-product, is separately prepared at ambient temperature and slowly added to the hot polymeric acid solution with continuous vigorous mixing so as to prevent localized precipitation of the cationic polymeric salt. .After addition is complete, mixing is continued to ensure that all the salt forming compound is reacted with the copolymer.
- an aqueous solution containing the zinc and/or strontium and preferably at least one other cation source is preheated to 70°-80°C. with vigorous stirring to form a homogeneous slurry.
- the lower alkyl vinyl ether-maleic acid copolymer (I) or its corresponding anhydride is then added to the slurry while further heating to 90°C. and stirring to ensure complete hydrolysis.
- reaction batch is then dried such as by shallow drying trays in a convection oven maintained at about 70°C. with hot air circulation to evaporate the water content and recover the polymeric salt product in dry form.
- reaction batch is then transferred to 5 drum dryers maintained at 80-100 PSIG with hot steam to evaporate the water content and recover the polymeric salt in the flake form.
- the resulting flakes may be subjected to milling and screening to yield the desired physical properties to provide satisfactory denture stabilizing properties.
- the salts are friable so that appropriate particle size and bulk density can be obtained. For best results, particles should be capable of passage through a 140- to 200-mesh sieve (U.S.B.S. series) and preferably are less than 0.74 millimeter in their largest dimension.
- the subject zinc and/or strontium AVE/MA copolymer salts have exceptional adhesive qualities when contacted with water or saliva such that they are extremely useful as denture adhesive materials in denture stabilizing compositions.
- the salt in particulate form is preferably characterized by a particle size of at least minus 140-mesh U.S.B.S. sieve; a bulk density greater than 0.3 gram per cubic centimeter and preferably higher than 0.6 gram per cubic centimeter; and a pH between 3 and 7.0, the pH being determined on a one percent by weight dispersion in water.
- Each of the subject zinc and/or strontium AVE/MA copolymer salts may be utilized in effective adhesive amounts, preferably at least 20 percent by weight, as the sole adhesive component or as a co-adhesive in joint usage with other active adhesive components in denture stabilizing compositions. Additionally, the subject zinc and/or strontium AVE/MA copolymer salts preferably contain other cations such as calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof.
- compositions also comprise polyethylene glycol.
- polyethylene glycols are polymers with the general formula (OCH2CH2)nOH, where n is greater than or equal to 4.
- the polyethylene glycols are designated by a number that represents the average molecular weight [Merck Index. Tenth Edition, No. 7441, 1983].
- the present compositions comprise polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600.
- Preferred is polyethylene glycol having an average molecular weight of equal to or greater than about 300 and equal to or below about 600.
- Polyethylene glycol having an average molecular weight of about 400 is most preferred.
- the polyethylene glycols suitable for use in the present invention are well known and commercially available, such as those marketed by Union Carbide Corporation under the trademark "Carbowax".
- polyethylene glycol that is useful in the present invention is based on compositions containing AVE/MA copolymer salts characterized by a particle size of at least minus 140-mesh U.S.B.S. sieve. Therefore, polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600 is present at a level of from about 20% to about 90%, preferably from about 30% to about 80% and most preferably from about 35% to about 75%, by weight of the invention compositions.
- Optional Components are examples of polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600.
- compositions may also include a safe and adhesively effective amount of a co-adhesive.
- safe and adhesively effective amount means an amount sufficient to provide adherence of a denture or dental prosthesis to the oral cavity.
- Preferred co-adhesives include a water-soluble hydrophilic colloid or polymer having the property of swelling upon exposure to moisture to form a mucilaginous mass.
- adhesive materials include natural gums, synthetic polymeric gums, adhesive materials commonly employed in denture stabilizing compositions and compatible with the subject AVE/MA copolymer salts, synthetic polymers, saccharide derivatives, cellulose derivatives, and mixtures thereof.
- -adhesives examples include karaya gum, guar gum, gelatin, algin, sodium alginate, tragacanth, methylcellulose, acrylamide polymers, ethylene oxide polymers, polyvinylpyrrolidone, cationic polyarylamide polymers, carboxymethylcellulose, sodium carboxymethylcellulose, and mixed partial salts of poly(vinyl methyl-ether maleate).
- Sodium carboxymethylcellulose is most preferred for use in the present invention.
- the -adhesives may be present at a level of from about 5% to about 70% by weight of the composition.
- colorants include colorants, preservatives such as methyl and propyl parabens; thickeners such as silicon dioxide, and polyethylene glycol having an average molecular weight of 8000; and vehicles such as liquid petrolatum, petrolatum, mineral oil and glycerin. Preferred are polyethylene glycol having an average molecular weight of 8000, silicon dioxide, and petrolatum. Colorants, preservatives, thickeners and vehicles may be present at levels of from about 0% to about 20%, by weight of the composition.
- compositions of the present invention may also include from about 0.01% to about 5% of one or more components which provide the user with sensory, including flavor, benefits.
- suitable components include natural or artificial sweetening agents, menthol, methyl lactate, wintergreen oil, peppermint oil, spearmint oil, leaf alcohol, as well as coolants 3-l-menthoxypropane-l,2-diol and paramenthane carboxyamide agents such as N-ethyl-p-menthane-3-carboxamide which is described in U.S. Patent 4,136,163 to Watson et. al., which is incorporated by reference herein in its entirety.
- compositions of the present invention are manufactured in an art- recognized manner known to those skilled in the art, such as powder, cream, ointment, liquid, or paste formulations. Suitable examples of such formulations are disclosed in U.S. Patent 4,518,721, issued May 21, 1985, and U.S. Patent 4,514,528, issued April 30, 1985, both to Dhabar et al., and both incorporated by reference herein in their entirety.
- the following non-limiting examples illustrate embodiments of the subject invention wherein both essential and optional ingredients are combined. These examples are given solely for the purpose of illustration and are not to be construed as limiting the scope of the invention.
- Polyethylene Glycol 400 41.0 37.0 33.1 39.5
- Examples I-IV are prepared as follows. Combine polyethylene glycol 400, petrolatum, (and mineral oil if present) and heat to about 55°-65°C until liquid.
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Abstract
The subject invention encompasses adhesive compositions comprising mixed partial salts of a lower alkyl vinyl ether-maleic acid copolymer and polyethylene glycol having an average molecular weight of above about 100 and equal to or below about 600.
Description
DENTURE STABILIZING COMPOSITIONS
BACKGROUND Ordinary removable dentures, dental plates and the like, comprise teeth mounted in a suitable plate or base. Although dentures generally are skillfully prepared, often they do not fit perfectly. Moreover, no matter how satisfactory at first, after a period of time the fit of the denture becomes loose and imperfect due to natural shrinkage and changes in the gums, mucous tissues, and the like. Loose and imperfectly fitted dentures usually are corrected and stabilized by the use of a denture stabilizer. Denture stabilizers are used to fill the interstices between the dentures and the gums or tissues. Prior to placement of the denture in the oral cavity, a denture stabilizer is applied to the denture-plate surface which, for a perfect fit, should uniformly contact the gums and mucous tissues. The denture stabilizer is formulated not only for its adherent properties, but also to provide a cushion or gasket between the denture and the gums or tissues, thereby positioning the denture securely in the oral cavity.
Several deficiencies that commonly exirt with denture stabilizing or adhesive compositions are phase separation, the need for more than one application of the adhesive per day and oozing of the adhesive from under the dental plate. Oozing is particularly undesirable because of the resulting unpleasant taste, unpleasant mouthfeel, and loss of adhesive from under the dental plate.
Considerable effort has been made over the years to develop improved denture adhesive compositions. Both synthetic and natural polymers and gums have been used singly, in combination, and in combination with various adhesives in an attempt to lessen the deficiencies noted above. However, the need still exists for improved denture stabilizing compositions which offer a secure hold, are aesthetically pleasing to the user, ooze less than currently available products, and are easy to clean from .the mouth and/or denture.
It has been discovered, in accordance with the present invention, that a denture stabilizer can be formulated having excellent adhesive quality while ooang less and providing pleasing aesthetics to the user. The invention adhesive compositions may also be effectively used as a wound dressing, underwater adhesive, bio-adhesive, and/or as a delivery vehicle for other actives.
It is an object of the present invention to provide a hydrophilic denture stabilizing composition which effectively holds dentures in place for prolonged periods of time yet allows for easy removal of the denture on demand. It is also an object of the invention to provide an improved denture stabilizing composition which oozes less than currently available stabilizers and is aesthetically pleasing to the user. It is a further object that the hydrophilic nature of the invention compositions will provide adhesive compositions that are easier to clean from the mouth and/or denture than currently available products.
These and other objects of the present invention will become readily apparent from the detailed description which follows.
SUMMARY OF THE INVENTION
The present invention encompasses adhesive compositions comprising: a) from about 10% to about 80% of a mixed partial salt of a lower alkyl vinyl ether- maleic acid copolymer consisting essentially of the repeated structural unit:
wherein R represents a Cl to C4 alkyl radical, n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 2SC, and wherein the partial salt contains a cationic salt function of from about 0.1% to about 65% zinc or strontium cations or mixtures thereof, of the total initial carboxyl groups reacted; and b) from about 20% to about 90% of polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600.
DETAILED DESCRIPTION OF THE INVENTION The adhesive compositions of the present invention comprise the mixed partial salt of a lower alkyl vinyl ether-maleic acid copolymer consisting of zinc and/or strontium salts, and polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600. Polyethylene glycol having an average molecular weight of about 400 is most preferred for use in the present
invention compositions. The present compositions may be formulated as creams, pastes, powders, liquids, ointments, and lotions. A detailed description of essential and optional components of the present invention is given below. Lower Alkyl Vinyl Ether-Maleic Acid Copolymer Salts
The present adhesive compositions comprise the mixed partial salt of a lower alkyl vinyl ether-maleic acid ("AVE/MA") copolymer consisting essentially of the repeated structural unit:
wherein R represents a Cl to C4 alkyl radical, n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 25C, and wherein the partial salts contain a cationic salt function of from about 0.1% to about 65% zinc and/or strontium cations, preferably from about 10% to about 45%, and most preferably from about 15% to about 30%, of the total initial carboxyl groups reacted. The term "mixed partial salt" as used herein refers to «zinc and/or strontium partial salts of lower alkyl vinyl ether-maleic acid copolymers where the zinc and strontium are mixed on the same copolymer with each other or with other ester functions or nonidentical cations selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof. Preferred are mixed partial copolymer salts containing zinc and calcium cations.
In the present invention compositions, the cationic salt function preferably further consists of from about 0.1% to about 75% metal salts selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof. Most preferred of the additional metal salts are calcium or sodium metal salts or mixtures thereof. Calcium cations may be present at a level of from about 10% to about 75%, preferably from about 25% to about 60%, and most preferably from about 40% to about 60%, of the total initial carboxyl groups reacted. Sodium cations may be present at a level of from about 1% to about 20%,
preferably from about 1% to about 15%, and most preferably from about 1% to about 10%, of the total initial carboxyl groups reacted.
The subject polymeric salts are advantageously prepared by the interaction of the AVE/MA copolymer (I) with cationic zinc and/or strontium compounds and preferably at least one calcium, sodium, magnesium, potassium, or ammonium compound having a functional group typical of reactants of a carboxylic acid, such as, for example, the hydroxide, acetate, halide, lactate, etc. in an aqueous medium. In a preferred embodiment, the oxide of anc .and the hydroxide of calcium are utilized. Since zinc hydroxide is not commercially available, its use as a reactant is readily and more economically accomplished by employing an aqueous slurry of particular zinc oxide which, although practically insoluble in water, provides hydration to zinc hydroxide on the paniculate surface. Strontium hydroxide, on the other hand, is available in either crystalline or powder form and is soluble in about 50 parts water. Aqueous solutions of strontium oxide, however, which forms the hydroxide when treated with water (caution: heat evolution), may also be used.
Anions that form toxic, irritating or contaminating by-products should be avoided, or special precautions and treatment provided to assure the removal and absence of such by-products from the polymeric salt end-product. The particular compound used should be substantially pure to assure obtaining a substantially pure, substantially off-white polymeric .salt end-product.
The lower alkyl vinyl ether maleic acid (AVE/MA) copolymers are readily obtained by copolymerizing a lower alkyl vinyl ether monomer, such as methyl vinyl ether, ethyl vinyl ether, divinyl ether, propyl vinyl ether and isobutyl vinyl ether, with maleic anhydride to yield the corresponding lower alkyl vinyl ether-maleic anhydride copolymer which is readily hydrolyzable to the acid copolymer (I). Both anhydride and acid forms are also available from commercial suppliers. For example, the GAF Corporation, Wayne, N.J. provides both the polymeric free acid form (I) and the corresponding anhydride form under its "GANTREZ" trademark as the "GANTREZ S Series" and "GANTREZ AN Series", respectively. In the former acid series, the GANTREZ S-97 (M. W. TM 50,000) is particularly suitable, and, in the latter anhydride series, the GANTREZ AN-149 (M. W. = 50,000) the GANTREZ AN-169 (M. W. = 67,000) and the GANTREZ AN-179 (M. W. = 80,000) copolymers are particularly suitable. The acid and anhydride forms of AVE/MA copolymers, having an average molecular weight of from about 50,000 to about 80,000 (as measured by membrane osmometry in 2-butanone 1-10 grams/ 1000 ml solution), are also characterized by having the previously described specific viscosity parameter of more than 1.2. When the anhydride copolymer
dissolves in water, the anhydride linkage is cleaved so that the highly polar, polymeric free acid (I) is formed. Accordingly, the anhydride form, which is relatively less expensive than the acid form, may be used as a convenient and cheaper precursor for the acid. Elevated temperatures may be advantageously employed to enhance the rate of anhydride-to-acid hydrolysis.
In general, the lower alkyl vinyl ether-maleic acid copolymer (I), or its corresponding anhydride, is added to water preheated to about 70°-80°C. with vigorous stirring to form a homogeneous mixture. If the anhydride precursor is utilized, it is recommended that the aqueous mixture be further heated to about 90° C. with stirring to ensure complete hydrolysis of the anhydride to the acid form. Heating is then discontinued although mixing is continued until the batch turns clear with a simultaneous decrease in viscosity (about 65°-75°C.). An aqueous solution of the cationic zinc and/or strontium salt forming compound, or, for example, an aqueous dispersion of paniculate zinc oxide is combined with calcium hydroxide in the form of a slurry, in an amount sufficient to provide the desire cationic content desired in the end-product, is separately prepared at ambient temperature and slowly added to the hot polymeric acid solution with continuous vigorous mixing so as to prevent localized precipitation of the cationic polymeric salt. .After addition is complete, mixing is continued to ensure that all the salt forming compound is reacted with the copolymer.
Alternatively, an aqueous solution containing the zinc and/or strontium and preferably at least one other cation source is preheated to 70°-80°C. with vigorous stirring to form a homogeneous slurry. The lower alkyl vinyl ether-maleic acid copolymer (I) or its corresponding anhydride is then added to the slurry while further heating to 90°C. and stirring to ensure complete hydrolysis.
The reaction batch is then dried such as by shallow drying trays in a convection oven maintained at about 70°C. with hot air circulation to evaporate the water content and recover the polymeric salt product in dry form. Alternatively, the reaction batch is then transferred to 5 drum dryers maintained at 80-100 PSIG with hot steam to evaporate the water content and recover the polymeric salt in the flake form.
The resulting flakes may be subjected to milling and screening to yield the desired physical properties to provide satisfactory denture stabilizing properties.
The salts are friable so that appropriate particle size and bulk density can be obtained. For best results, particles should be capable of passage through a 140- to 200-mesh sieve (U.S.B.S. series) and preferably are less than 0.74 millimeter in their largest dimension.
The subject zinc and/or strontium AVE/MA copolymer salts have exceptional adhesive qualities when contacted with water or saliva such that they are extremely useful as denture adhesive materials in denture stabilizing compositions. For such use the salt in particulate form is preferably characterized by a particle size of at least minus 140-mesh U.S.B.S. sieve; a bulk density greater than 0.3 gram per cubic centimeter and preferably higher than 0.6 gram per cubic centimeter; and a pH between 3 and 7.0, the pH being determined on a one percent by weight dispersion in water.
Each of the subject zinc and/or strontium AVE/MA copolymer salts may be utilized in effective adhesive amounts, preferably at least 20 percent by weight, as the sole adhesive component or as a co-adhesive in joint usage with other active adhesive components in denture stabilizing compositions. Additionally, the subject zinc and/or strontium AVE/MA copolymer salts preferably contain other cations such as calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof. Polyethylene Glvcol
The invention compositions also comprise polyethylene glycol. In general, polyethylene glycols are polymers with the general formula (OCH2CH2)nOH, where n is greater than or equal to 4. The polyethylene glycols are designated by a number that represents the average molecular weight [Merck Index. Tenth Edition, No. 7441, 1983].
The present compositions comprise polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600. Preferred is polyethylene glycol having an average molecular weight of equal to or greater than about 300 and equal to or below about 600. Polyethylene glycol having an average molecular weight of about 400 is most preferred. The polyethylene glycols suitable for use in the present invention are well known and commercially available, such as those marketed by Union Carbide Corporation under the trademark "Carbowax".
The level of polyethylene glycol that is useful in the present invention is based on compositions containing AVE/MA copolymer salts characterized by a particle size of at least minus 140-mesh U.S.B.S. sieve. Therefore, polyethylene glycol having an average molecular weight above about 100 and equal to or below about 600 is present at a level of from about 20% to about 90%, preferably from about 30% to about 80% and most preferably from about 35% to about 75%, by weight of the invention compositions. Optional Components
The present invention compositions may also include a safe and adhesively effective amount of a co-adhesive. The term "safe and adhesively effective amount"
as used herein means an amount sufficient to provide adherence of a denture or dental prosthesis to the oral cavity.
Preferred co-adhesives include a water-soluble hydrophilic colloid or polymer having the property of swelling upon exposure to moisture to form a mucilaginous mass. Such adhesive materials include natural gums, synthetic polymeric gums, adhesive materials commonly employed in denture stabilizing compositions and compatible with the subject AVE/MA copolymer salts, synthetic polymers, saccharide derivatives, cellulose derivatives, and mixtures thereof. Examples of such materials include karaya gum, guar gum, gelatin, algin, sodium alginate, tragacanth, methylcellulose, acrylamide polymers, ethylene oxide polymers, polyvinylpyrrolidone, cationic polyarylamide polymers, carboxymethylcellulose, sodium carboxymethylcellulose, and mixed partial salts of poly(vinyl methyl-ether maleate). Sodium carboxymethylcellulose is most preferred for use in the present invention. In general, the -adhesives may be present at a level of from about 5% to about 70% by weight of the composition.
Other suitable optional ingredients include colorants, preservatives such as methyl and propyl parabens; thickeners such as silicon dioxide, and polyethylene glycol having an average molecular weight of 8000; and vehicles such as liquid petrolatum, petrolatum, mineral oil and glycerin. Preferred are polyethylene glycol having an average molecular weight of 8000, silicon dioxide, and petrolatum. Colorants, preservatives, thickeners and vehicles may be present at levels of from about 0% to about 20%, by weight of the composition.
The compositions of the present invention may also include from about 0.01% to about 5% of one or more components which provide the user with sensory, including flavor, benefits. Suitable components include natural or artificial sweetening agents, menthol, methyl lactate, wintergreen oil, peppermint oil, spearmint oil, leaf alcohol, as well as coolants 3-l-menthoxypropane-l,2-diol and paramenthane carboxyamide agents such as N-ethyl-p-menthane-3-carboxamide which is described in U.S. Patent 4,136,163 to Watson et. al., which is incorporated by reference herein in its entirety.
The compositions of the present invention are manufactured in an art- recognized manner known to those skilled in the art, such as powder, cream, ointment, liquid, or paste formulations. Suitable examples of such formulations are disclosed in U.S. Patent 4,518,721, issued May 21, 1985, and U.S. Patent 4,514,528, issued April 30, 1985, both to Dhabar et al., and both incorporated by reference herein in their entirety.
The following non-limiting examples illustrate embodiments of the subject invention wherein both essential and optional ingredients are combined. These examples are given solely for the purpose of illustration and are not to be construed as limiting the scope of the invention.
EXAMPLES I-rV
Ingredients Weight Percentages
47.5% Calcium/17.5% Zinc mixed partial I π πι IV salt of AVE/MA copolymer a) 31.5 32.0 30.8 29.5
Polyethylene Glycol 400 41.0 37.0 33.1 39.5
Sodium Carboxymethylcellulose 18.5 18.0 20.2 19.7
Petrolatum 8.0 8.0 15.9 7.8
Polyethylene Glycol 8000 1.0 0.0 0.0 3.5
Mineral Oil 0.0 5.0 0.0 0.0
Silicon Dioxide 0.0 1.0 0.0 0.0
(a) AVE/MA copolymer having about 47.5% neutralization with calcium and about 17.5% neutralization with zinc.
Examples I-IV are prepared as follows. Combine polyethylene glycol 400, petrolatum, (and mineral oil if present) and heat to about 55°-65°C until liquid.
Add sodium carboxymethylcellulose, AVE/MA copolymer salt, (and polyethylene glycol 8000 and silicon dioxide if present). Stir until well mixed. Cool to room temperature.
Claims
What is claimed is:
An adhesive composition comprising: a) from 10% to 80% of a mixed partial salt of a lower alkyl vinyl ether- maleic acid copolymer consisting essentially of the repeated structural unit:
wherein R represents a Cl to C4 alkyl radical, n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 25°C, and wherein the partial salts contain a cationic salt function of from 0.1% to 65% zinc or strontium cations or mixtures thereof, of the total initial carboxyl groups reacted; and b) from 20% to 90% of polyethylene glycol having an average molecular weight above 100 and equal to or below 600.
2. The composition according to Claim 1 wherein the cationic salt function further consists of from 0.1% to 75% metal salts selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof.
3. The composition according to Claim 2 comprising from 20% to 90% of polyethylene glycol having an average molecular weight of equal to or greater than 300 and equal to or below 600.
4. An adhesive composition comprising: a) from 20% to 70% of a mixed partial salt of a lower alkyl vinyl ether- maleic acid copolymer consisting essentially of the repeated structural unit:
wherein R represents a Cl to C4 alkyl radical, n is an integer greater than one representing the number of repeated occunences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 25°C, and wherein the partial salts contain a cationic salt function of from 0.1% to 65% zinc or strontium cations or mixtures thereof, of the total initial carboxyl groups reacted ; and b) from 30% to 80% of polyethylene glycol having an average molecular weight above 100 and equal to or below 600.
5. The composition according to Claim 4 wherein (a) is zinc and strontium.
6. The composition according to Claim 4 wherein the cationic salt function further consists of from 0.1% to 75% metal salts selected from the group consisting of calcium, sodium, magnesium, potassium, ammonium, and mixtures thereof.
7. The composition according to Claim 6 comprising from 30% to 80% of polyethylene glycol having an average molecular weight equal to or greater than 300 and equal to or below 600.
8. The composition according to Claim 7 which further comprises from 10% to 75% calcium cations.
9. The composition according to Claim 8 further comprising optional components selected from the group consisting of colorants, preservatives, thickeners, vehicles, and mixtures thereof.
10. The composition according to Claim 8 further comprising a safe and adhesively effective amount of a co-adhesive selected from the group consisting of natural gums, synthetic polymeric gums, synthetic polymers, saccharide derivatives, cellulose derivatives, and mixtures thereof.
11. .An adhesive composition comprising: a) from 25% to 65% of a mixed partial salt of a lower alkyl vinyl ether- maleic acid copolymer consisting essentially of the repeated structural unit:
wherein R represents a Cl to C4 alkyl radical, n is an integer greater than one representing the number of repeated occurrences of the structural unit in a molecule of the copolymer and n is large enough to characterize the copolymer as having a specific viscosity larger than 1.2, the specific viscosity being determined in methyl ethyl ketone at 25°C, and wherein the partial salts contain a cationic salt function of from 15% to 30% zinc cations; from 25% to 60% calcium cations, of the total initial carboxyl groups reacted; and b) from 35% to 75% of polyethylene glycol having an average molecular weight of 400.
12. The composition according to Claim 11 further comprising optional components selected from the group consisting of colorants, preservatives, thickeners, vehicles, and mixtures thereof.
13. The composition according to Claim 12 further comprising a safe and adhesively effective amount of a co-adhesive selected from the group consisting of natural gums, synthetic polymeric gums, synthetic polymers, saccharide derivatives, cellulose derivatives, and mixtures thereof.
14. The composition according to Claim 11 wherein the partial salt further comprises a cationic salt function of from 1% to 20% sodium cations.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25761794A | 1994-06-09 | 1994-06-09 | |
| US257617 | 1994-06-09 | ||
| PCT/US1995/007282 WO1995033435A1 (en) | 1994-06-09 | 1995-06-07 | Denture stabilizing compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0764013A1 true EP0764013A1 (en) | 1997-03-26 |
Family
ID=22977019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP95923006A Withdrawn EP0764013A1 (en) | 1994-06-09 | 1995-06-07 | Denture stabilizing compositions |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0764013A1 (en) |
| JP (1) | JPH10501243A (en) |
| AU (1) | AU2769495A (en) |
| CA (1) | CA2192322A1 (en) |
| WO (1) | WO1995033435A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5696181A (en) * | 1995-09-22 | 1997-12-09 | The Block Drug Company, Inc. | Denture fixative |
| DE69927392T2 (en) * | 1998-09-30 | 2006-07-06 | Block Drug Co., Inc. | DENTAL PROSTHESIS ADHESIVE |
| US6110989A (en) * | 1998-09-30 | 2000-08-29 | Block Drug Company, Inc. | Denture adhesive |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4514528A (en) * | 1983-02-16 | 1985-04-30 | Richardson-Vicks Inc. | Hydrophilic denture adhesive |
| US5073604A (en) * | 1989-05-04 | 1991-12-17 | Richardson-Vicks, Inc. | Denture stabilizing compositions |
| BR9107175A (en) * | 1990-12-21 | 1994-02-08 | Richardson Vicks Inc | DENTAL STABILIZING COMPOSITES HAVING IMPROVED RETENTION |
-
1995
- 1995-06-07 AU AU27694/95A patent/AU2769495A/en not_active Abandoned
- 1995-06-07 EP EP95923006A patent/EP0764013A1/en not_active Withdrawn
- 1995-06-07 WO PCT/US1995/007282 patent/WO1995033435A1/en not_active Ceased
- 1995-06-07 JP JP8501305A patent/JPH10501243A/en active Pending
- 1995-06-07 CA CA002192322A patent/CA2192322A1/en not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9533435A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1995033435A1 (en) | 1995-12-14 |
| AU2769495A (en) | 1996-01-04 |
| JPH10501243A (en) | 1998-02-03 |
| CA2192322A1 (en) | 1995-12-14 |
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