Dental calculus inhibiting compositions

Claim 2

An oral composition comprising: (a) an effective amount of a fluoride source, (b) effective amount of a dental abrasive; and (c) 0.01 to 10% by weight of an anticalculus agent selected from homopolymers of monounsaturated monocarboxylic and dicarboxylic acids of 3 to 5 carbon atoms, salts and anhydrides thereof, and from copolymers containing at least 30% by weight of a carboxylic monomer selected from said acids, and mixtures of such anticalculus agents.

Claim 3

Composition of claim 1 wherein at least one comonomer of said copolymer is selected from acrylamides, alkyl acrylates, alkyl itaconates, vinyl sulfonic acid, hydroxyalkyl acrylates, alkoxyalkyl acrylates, loweralkenyl carboxylates, styrene sulfonic acids, allyloxyhydroxyalkane sulfonic acids, acrylamidoalkane sulfonic acids, phosphonoalkane carboxylic acids, sulfoalkyl acrylates, salts and anhydrides thereof, and mixtures of such comonomers.

Claim 4

Composition of claim 2 wherein amount of said fluoride source is 0.005 to 3.0% by weight of said oral composition, wherein amount of said carboxylic monomer is 40 to 90% in said copolymers, and wherein molecular weight of said homopolymers and said copolymers is in the range of about 400 to 100,000.

Claim 5

Composition of claim 3 wherein said copolymer contains 60 to 10% of at least one of said comonomers, wherein amount of said fluoride source is 0.05 to 1%, and wherein amount of said anticalculus agent is 0.1 to 5%.

Claim 6

Composition of claim 5 wherein said carboxylic monomer is selected from acrylic acid, methacrylic acid, itaconic acid, maleic acid and its anhydride, citraconic acid, mesaconic acid, salts of such acids, and mixtures thereof; where acrylamides are defined as follows: ##STR15## where R is selected from hydrogen and methyl groups; and R 1 and R 2 are individually selected from hydrogen and alkyl groups of 1 to 12 carbon atoms; where alkyl acrylates are defined as follows: ##STR16## where R is selected from hydrogen and methyl groups and R 1 is selected from alkyl groups of 1 to 6 carbons and substituted alkyl groups where R' is defined as R 2 is an alkyl group of 1 to 6 carbons and Y is selected from SO 3 X, --COR 3 , and --CO 2 X where Y is selected from hydrogen, alkali metals alkaline earth metals, and ammonium groups and R.sup. 3 is selected from alkyl groups of 1 to 3 carbons; where alkyl itaconates are defined as follows: ##STR17## where R 2 and R 3 are individually selected from hydrogen and alkyl groups of 1 to 4 carbon atoms provided that both R 2 and R 3 are not hydrogens although either R 2 or R 3 can be hydrogen; where vinyl sulfonic acid and salts thereof are defined as follows: ##STR18## where X is selected from hydrogen, alkali metals, alkaline earth metals, and ammonium radicals; where hydroxyalkyl acrylates are defined as follows: ##STR19## where R is selected from hydrogen and alkyl groups of 1 to 3 carbons, R 1 is selected from alkylene groups of 2 to 4 carbons, and n is from 1 to 5; where alkoxyalkyl acrylates are defined as follows: ##STR20## where R is selected from hydrogen and methyl groups, R 1 is selected from alkylene groups of 2 to 4 carbons, R 2 is selected from alkyl groups 1 to 10 carbons, and n is from 1 to 5; where lower alkenyl carboxylates are defined as follows: ##STR21## where R is hydrogen or a lower alkyl group of 1 to 6 carbon atoms, and R 1 is selected from alkyl groups of 1 to 12 carbon atoms; where vinyl alcohol is defined as follows: ##STR22## where R is hydrogen or a lower alkyl group of 1 to 6 carbon atoms; where styrene sulfonic acids and salts thereof are defined as follows: ##STR23## where R is selected from hydrogen and alkyl groups of 1 to 6 carbons, and X is selected from hydrogen, alkali metals, alkaline earth metals and ammonium radicals; where allyloxy hydroxyalkane sulfonic acids and salts thereof are defined as follows: ##STR24## where R and R 1 are individually selected from hydrogen and methyl groups, and X is selected from hydrogen, alkali metals, alkaline earth metals, and ammonium radicals; where acrylamidoalkane sulfonic acids and salts thereof are defined as follows: ##STR25## where R is selected from hydrogen and methyl groups, R 1 and R 2 are individually selected from hydrogen and alkyl groups of 1 to 4 carbons, X is selected from hydrogen, alkali metals, alkaline earth metals, and ammonium radicals; and where sulfoalkyl acrylates are defined as follows: ##STR26## where R 1 is selected from hydrogen, methyl, and the group defined as ##STR27## where R 2 is selected from alkylene groups of 1 to 12 carbon atoms and X is selected from hydrogen, alkali metals, alkaline earth metals, and ammonium radicals.

Claim 7

Composition of claim 5 wherein said acrylamides, both R 1 or R 2 are not hydrogens; where in said alkyl acrylates, R 1 is selected from unsubstituted alkyl groups of 1 to 4 carbons; where in said alkyl itaconates R 2 and R 3 are individually selected from unsubstituted alkyl groups of 1 to 4 carbons; wherein said sulfonic acid and salts thereof, X is selected from alkali metals and ammonium radicals; where in said hydroxyalkyl acrylates, R is selected from hydrogen and methyl groups and R 1 is selected from alkylene group of 2 to 3 carbons; wherein said alkoxyalkyl acrylates, R 1 is selected from alkylene groups of 2 to 3 carbons, R 2 is selected from alkyl groups of 1 to 4 carbons, and n is from 1 to 3; where in said styrene sulfonic acids and salts thereof, R is hydrogen, X is selected from hydrogen, ammonium and alkali metal radicals, and said --SO 3 X group is located at the 3 or 4 position on said phenyl ring; wherein said acrylamidoalkane sulfonic acid and salts thereof, R is hydrogen and R 1 and R 2 are individually selected from alkyl groups of 1 to 3 carbons; and where in said sulfoalkyl acrylates, R 2 is selected from alkylene groups of 2 to 4 carbons and X is selected from hydrogen, sodium, potassium, calcium, magnesium, and ammonium radicals.

Claim 8

Composition of claim 6 having pH of 6 to 10 which is effective in inhibiting formation of dental calculus wherein amount of said fluoride source is sufficient to supply from about 50 ppm to about 2,500 ppm of fluoride ions; wherein amount of said anticalculus agent is 1 to 1000 ppm; wherein amount of said dental abrasive is 10 to 70%; and wherein said composition also includes an oral vehicle.

Claim 9

Composition of claim 7 wherein amount of said abrasive is 0.1 to 7% by weight of a polyphosphate selected from alkali metal hexammetaphosophate, alkali metal tripolyphosphate, dialkali metal diacid, trialkali metal monoacid, alkali metal tripolyphosphate, tetraalkali metal pyrophosphate, hydroxyethylethane diphosphonic acid, and mixtures thereof.

Claim 10

Composition of claim 6 wherein amount of said calculus agent is 1 to 55, said copolymeric anticalculus agents have molecular weight of 2,000 to 20,000 and said monounsaturated carboxylic acid is selected from acrylic acid, methacrylic acid, maleic acid or its anhydride, itaconic acid, and mixtures thereof.

Claim 11

Composition of claim 9 wherein said anticalculus agent is selected from the following copolymers: (a) 60:20:20 copolymer of AA:MAA:t-BuAm (b) 63:37 copolymer of AA:HPA (c) 51:49 copolymer of AA:AMPS (d) 100 homopolymer of maleic acid (e) 100 homopolymer of acrylic acid wherein the contractions used above are defined as follows: AA=acrylic acid MAA=methacrylic acid HPA=hydroxypropyl acrylate AMPS=2-acrylamido-2-methylpropane sulfonic acid.

Claim 12

Composition of claim 5 in toothpaste form wherein said fluoride source is selected from sodium fluoride, stannous fluoride, sodium monofluorophosphate, and mixtures thereof; amount of said dental abrasive is 10 to 75% and said dental abrasive is selected from silica, hydrated aluminum, insoluble metaphosphates, thermosetting polymerized resins, and mixtures thereof; and amount of said oral vehicle is 10 to 90% by weight.

Claim 13

Method of inhibiting dental calculus comprising applying to oral cavity composition as defined in claim 1.

Claim 14

Method of inhibiting dental calculus comprising applying to oral cavity composition as defined in claim 3.

Claim 15

Method of inhibiting dental calculus comprising applying to teeth composition as defined by claim 4.

Claim 16

Method comprising applying to teeth composition as defined by claim 5.

Claim 17

Method comprising applying to teeth composition as defined by claim 7.

Claim 18

Method comprising applying to teeth composition as defined by claim 11.