IP Library Granted Patent US 7,189,385
Granted Patent B2
US 7,189,385 · App. 10/715,917 · Granted Mar 13, 2007

Tooth whitening compositions

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Quick Facts
Patent No.
US 7,189,385
App. No.
10/715,917
Granted
Mar 13, 2007
Kind
B2
Abstract

Novel compositions and methods are disclosed for cosmetically treating teeth in a manner to increase brightness or shade of the teeth. The compositions include a low molecular weight compound having a high acetyl group functionality useful in the production of a peroxy acid which then acts as a whitening agent.

Claims (43)

1. A composition comprising:

an orally acceptable, tooth whitening peroxyacetic acid generating mixture including a source of hydrogen peroxide and an acetic acid ester of glycerin, wherein the source of hydrogen peroxide and the acetic acid ester of glycerin are dispersed within an orally acceptable anhydrous carrier further comprising a flavorant or sweetener, wherein said flavorant improves the palatability and oral acceptability of said composition.

2. The composition of claim 1 wherein the acetic acid ester of glycerin is selected from the group consisting of glyceryl triacetate, glyceryl diacetate and glyceryl acetate.

3. A composition according to claim 1 wherein the source of hydrogen peroxide is selected from the group consisting of carbamide peroxide, sodium percarbonate, sodium perborate, calcium peroxide, magnesium peroxide, sodium peroxide, and anhydrous poly(vinyl pyrrolidone)/hydrogen peroxide complexes.

4. A composition according to claim 1 capable of providing an oral pH of more than 5.2 to generate peroxyacetic acid.

5. A composition according to claim 4 , wherein the oral pH is 7.8.

6. The composition of claim 1 wherein the orally acceptable anhydrous carrier is selected from the group consisting of glycerin, propylene glycol, polyethylene glycols, chewing gum and gum base products, floss carriers and floss wax products, mineral oils, vegetable oils, waxes and esters.

7. The composition of claim 1 wherein the orally acceptable anhydrous carrier comprises a thickening agent.

8. The composition of claim 4 wherein the thickening agent is selected from the group consisting of neutralized carboxypolymethylene, polyacrylic acid polymers and copolymers, hydroxypropylcellulose and other cellulose ethers, salts of poly(methyl vinyl ether-co-maleic anhydride), poly(vinylpyrrolidone), poly(vinylpyrrolidone-co-vinyl acetate), silicon dioxide, fumed silica, and stearic acid esters.

9. The composition of claim 1 wherein the orally acceptable anhydrous carrier comprises a buffer.

10. The composition of claim 9 wherein the buffer is selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium phosphate di- and tn-basic, potassium phosphate di- and tri-basic, sodium tripolyphosphate, tris (hydroxymethyl) aminomethane, triethanolamine, polyethylenimine, polyacrylic acid, poly (methyl vinyl ether-co-maleic anhydride), citric acid, and phosphoric acid.

11. The composition of claim 1 wherein the orally acceptable anhydrous carrier comprises a surfactant.

12. The composition of claim 11 wherein the surfactant is selected from the group consisting of zwitterionic and fluorinated surfactants.

13. The composition of claim 1 wherein the orally acceptable anhydrous carrier comprises a chelating agent.

14. The composition of claim 13 wherein the chelating agent is selected from the group consisting of phosphonic acids, EDTA, and polyphosphates.

15. A method for whitening teeth comprising:

applying one of either a glyceryl triacetate or a source of hydrogen peroxide onto a tooth surface; and

applying the other of the remaining glyceryl triacetate or source of hydrogen peroxide onto the same tooth surface, so as to generate peroxyacetic acid upon contact with an aqueous solution on the surface of the tooth.

16. A method for cosmetically treating teeth comprising the steps of:

applying a C1–C5 molecule having between 1 to 5 labile C1–C5 acetyl containing groups onto the surface of a tooth;

allowing the C1–C5 molecule having between 1 to 5 labile C1–C5 acetyl containing groups to penetrate into the tooth;

applying a source of peroxide onto the surface of the tooth; allowing the C1–C5 molecule having between 1 to 5 labile C1–C5 acetyl containing groups to react with the source of hydrogen peroxide to generate a peroxyacid within the tooth; and

allowing the peroxyacid to effect whitening of the tooth.

17. The method of claim 16 wherein the C1–C5 molecule having between 1 to 5 labile C1–C5 acetyl containing groups has a molecular weight of between about 100 to about 300.

18. The method of claim 16 wherein the C1–C5 molecule having between 1 to 5 labile C1–C5 acetyl containing groups has a molecular weight approximate that of glyceryl triacetate.

19. A composition for whitening teeth in an oral cavity comprising:

a source of hydrogen peroxide in an amount that results in about 0.1% to about 15.0% of hydrogen peroxide when applied to the oral cavity;

an acetic acid ester of glycerin in an amount of about 0.1% to about 6.0%; and

an orally acceptable anhydrous carrier in an amount of about 79.0% to about 99.8%;

wherein the percentages are weight to weight of the composition.

20. The composition of claim 19 wherein the acetic acid ester of glycerin is selected from the group consisting of glyceryl triacetate, glyceryl diacetate and glyceryl acetate.

21. A composition according to claim 19 , wherein the source of hydrogen peroxide is selected from the group consisting of carbamide peroxide, sodium percarbonate, sodium perborate, calcium peroxide, magnesium peroxide, sodium peroxide, and anhydrous poly(vinyl pyrrolidone)/hydrogen peroxide complexes.

22. The composition of claim 19 , wherein the orally acceptable anhydrous carrier is selected from the group consisting of glycerin, propylene glycol, polyethylene glycols, chewing gum and gum base products, floss carriers and floss wax products, mineral oils, vegetable oils, waxes and esters.

23. The composition of claim 19 , wherein the orally acceptable anhydrous carrier comprises a thickening agent in an amount of about 0.5% to about 20.0%.

24. The composition of claim 23 , wherein the thickening agent is selected from the group consisting of neutralized carboxypolymethylene, polyacrylic acid polymers and copolymers, hydroxypropylcellulose and other cellulose ethers, salts of poly(methyl vinyl ether-co-maleic anhydride), poly(vinylpyrrolidone), poly(vinylpyrrolidone-co-vinyl acetate), silicon dioxide, fumed silica, and stearic acid esters.

25. The composition of claim 19 , wherein the orally acceptable anhydrous carrier comprises a buffer in an amount of about 0.5% to about 3.0%.

26. The composition of claim 25 , wherein the buffer is selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium phosphate di- and tn-basic, potassium phosphate di- and tri-basic, sodium tripolyphosphate, tris(hydroxymethyl)aminomethane, triethanolamine, polyethylenimine, polyacrylic acid, poly(methyl vinyl ether-co-maleic anhydride), citric acid, and phosphoric acid.

27. The composition of claim 19 , wherein the orally acceptable anhydrous carrier comprises a surfactant in an amount of about 0.1% to about 2.0%.

28. The composition of claim 27 , wherein the surfactant is selected from the group consisting of zwitterionic and fluorinated surfactants.

29. The composition of claim 19 , wherein the orally acceptable anhydrous carrier comprises a chelating agent in an amount of about 0.01% to about 5.0%.

30. The composition of claim 29 , wherein the chelating agent is selected from the group consisting of phosphonic acids, EDTA, and polyphosphates.

31. The composition of claim 19 , wherein the orally acceptable anhydrous carrier comprises flavorants or sweeteners in an amount of about 0.05% to about 1.5%.

32. The composition of claim 20 , wherein the acetic acid ester of glycerin comprises glyceryl triacetate in an amount of about 6.0%.