IP Library Granted Patent US 6,837,712
Granted Patent B2
US 6,837,712 · App. 10/226,915 · Granted Jan 4, 2005

Dental restorative compositions

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Quick Facts
Patent No.
US 6,837,712
App. No.
10/226,915
Granted
Jan 4, 2005
Kind
B2
Abstract

A composition and a method of use as a dental restorative. A series of highly alkoxylated tri-functional monomers are used as a low viscosity monomer in a photo- or self-curable dental composition that resulted in low polymerization shrinkage. The mechanical strength of the restorative material was not compromised. The restorative composition may be used as a dental filling material, a cement, a liner/base, or an adhesive.

Claims (65)

1. A dental restorative composition comprising

(a) a first alkoxylated and trifunctional monomer of the formula

wherein G is an alkylene oxide unit, and 3≦x+y+z≦30 with the proviso that when G is ethylene oxide 3<x+y+z≦30, and R 1 , R 2 , and R 3 are ethylenically unsaturated groups,

(b) a second monomer comprising at least one ethylenically unsaturated group, and

(c) a polymerization initiator.

2. The dental restorative composition of claim 1 further comprising a finely divided filler.

3. The dental restorative composition of claim 2 wherein the filler is selected from the group consisting of inorganic metal, salt, oxide, silicate, aluminosilicate, aluminoborosilicate, fluoroaluminosilicate, colloidal silica, precipitated silica, polymeric filler, polymerized composite filler with inorganic particles, and combinations thereof.

4. The dental restorative composition of claim 2 wherein the filler is selected from the group consisting of bariumaluminosilicate, bariumaluminoborosilicate, strontiumaluminosilicate, zincaluminosilicate, bariumaluminofluorosilicate, strontiumaluminofluorosilicate, fumed silica, and combinations thereof.

5. The dental restorative composition of claim 2 wherein the filler has a mean particle size less than 15 microns.

6. The dental restorative composition of claim 2 wherein the filler has a mean particles size less than 5 microns.

7. The dental restorative composition of claim 2 wherein the filler has a mean particle size less than 2 microns.

8. The dental restorative composition of claim 2 wherein the filler comprises a nano-particle filler.

9. The dental restorative composition of claim 8 wherein the filler has a mean particle size in the range of about 5 nm to about 200 nm.

10. The dental restorative composition of claim 2 wherein the filler is surface treated or surface coated with a coupling agent.

11. The dental restorative composition of claim 10 wherein the coupling agent is γ-methacryloyloxypropyltrimethoxysilane.

12. The dental restorative composition of claim 1 wherein R 1 , R 2 , and R 3 are selected from the group consisting of

13. The dental restorative composition of claim 1 wherein x+y+z is in the range of 3 to 15.

14. The dental restorative composition of claim 1 wherein G is —OC n H 2n — and n is in the range between 1 and 12.

15. The dental restorative composition of claim 1 wherein G is a linear or branched alkylene oxide unit.

16. The dental restorative composition of claim 1 wherein the first monomer comprises a combination of at least two different tri-functional monomers and the mean (x+y+z) is ≧3 and ≦30.

17. The dental restorative composition of claim 1 wherein the first monomer comprises a combination of at least two different tri-functional monomers and the mean (x+y+z) is in the range of 3 to 15.

18. The dental restorative composition of claim 1 wherein the second monomer comprises at least two ethylenically unsaturated groups.

19. The dental restorative composition of claim 1 wherein the second monomer is selected from the group consisting of 2,2-bis[4-2(-hydroxy-3-methacryloylpropoxy)-phenyl]-propane (Bis-GMA), ethoxylated bisphenol A dimethacrylate (EBPADMA with 2 to 12 moles of ethylene oxide per molecule), the reaction product of 2-hydroxyethyl methacrylate with 2,4,4-trimethylhexane diisocyanate (UDMA), and triethylene glycol dimethacrylate (TEGDMA).

20. The dental restorative composition of claim 1 wherein the ethylenically unsaturated group of the second monomer is selected from the group consisting of methacrylate and acrylate.

21. The dental restorative composition of claim 1 wherein the polymerization initiator is selected from the group consisting of a photo initiator system, a redox initiator system, and combinations thereof.

22. The dental restorative composition of claim 21 wherein the photo-initiator system comprises a photo-sensitizer and an activator.

23. The dental restorative composition of claim 22 wherein the activator is a tertiary amine.

24. The dental restorative composition of claim 21 wherein the photo-sensitizer is camphorquinone.

25. The dental restorative composition of claim 21 wherein the redox initiator system comprises an oxidizing agent and a reducing agent.

26. The dental restorative composition of claim 25 wherein the oxidizing agent is a peroxide.

27. The dental restorative composition of claim 25 wherein the reducing agent is selected from the group consisting of a tertiary amine, a sulfinic acid, an alkali metal sulfinate, and combinations thereof.

28. The dental restorative composition of claim 1 wherein the composition is a one-part light-cure composition using a photo-initiator system.

29. The dental restorative composition of claim 1 wherein the composition is a two-part self-cure composition using a redox initiator system.

30. The dental restorative composition of claim 1 wherein the composition is a two-part dual-cure composition using a combined photo-initiator and redox initiator system.

31. The dental restorative composition of claim 1 further comprising a solvent selected from the group consisting of water, acetone, methanol, ethanol, isopropanol, and combinations thereof.

32. The dental restorative composition of claim 1 further comprising a stabilizer.

33. The dental restorative composition of claim 1 further comprising a ultraviolet stabilizer.

34. The dental restorative composition of claim 1 wherein the composition is selected from the group consisting of resin composite, a resin-ionomer, and a resin-modified glass-ionomer.

35. The dental restorative composition of claim 1 is a filling material, a cement, a liner, a base, an adhesive, or a combination thereof.

36. The method of using the dental restorative composition of claim 1 comprising applying the composition to the tooth, and hardening the composition.

37. A dental restorative composition comprising

(a) a first alkoxylated and trifunctional monomer of the formula

wherein G is selected from the group consisting of ethylene oxide, n-propylene oxide, isopropylene oxide, n-butylene oxide, and combinations thereof, 3≦x+y+z≦20 with the proviso that when G is ethylene oxide 3<x+y+z≦20, and R 1 , R 2 , and R 3 are independently selected from the group consisting of acrylate and methacrylate,

(b) a second monomer comprising at least two ethylenically unsaturated groups,

(c) a finely divided filler, and

(d) a polymerization initiator selected from the group consisting of a photo-initiator, a redox initiator, and combinations thereof.

38. The dental restorative composition of claim 37 wherein the filler has a mean particle size less than 15 microns.

39. The dental restorative composition of claim 37 wherein the second monomer is selected from the group consisting of 2,2-bis[4-2(-hydroxy-3-methacryloylpropoxy)-phenyl]-propane (Bis-GMA), ethoxylated bisphenol A dimethacrylate (EBPADMA with 2 to 12 moles of ethylene oxide per molecule), the reaction product of 2-hydroxyethyl methacrylate with 2,4,4-trimethylhexane diisocyanate (UDMA), and triethylene glycol dimethacrylate (TEGDMA).

40. The dental restorative composition of claim 37 is a filling material.

41. The dental restorative composition of claim 37 is a cement.

42. A dental restorative composition comprising

(a) a combination of at least two alkoxylated and trifunctional monomer of the formula

wherein G is an alkylene oxide unit and the mean (x+y+z) is in the range of 3 to 30 and R 1 , R 2 , and R 3 are ethylenically unsaturated groups,

(b) a second monomer comprising at least one ethylenically unsaturated group, and

(c) a polymerization initiator.

43. The composition of claim 42 further comprising a finely divided filler.

44. A method for providing a dental restorative composition, the composition comprising

(a) a first alkoxylated and trifunctional monomer of the formula

wherein G is an alkylene oxide unit, and 3≦x+y+z≦30 with the proviso that when G is ethylene oxide 3<x+y+z≦30, and R 1 , R 2 , and R 3 are ethylenically unsaturated groups,

(b) a second monomer comprising at least one ethylenically unsaturated group,

(c) a polymerization initiator,

(d) optionally, a finely divided filler,

applying the composition to the tooth and hardening the composition to reduce polymerization shrinkage.

45. The method of claim 44 wherein the composition is selected from the group consisting of a resin composite, a resin-ionomer, and a resin-modified glass ionomer.

46. The method of claim 44 wherein the composition is selected from the group consisting of a filling material, a cement, a liner, a base, and an adhesive.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 9, 2021
From: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
To: KERR CORPORATION
Reel/Frame 055886/0185 →
SECURITY INTEREST Recorded May 8, 2020
From: KERR CORPORATION
To: BANK OF AMERICA, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 052611/0362 →
CORRECTIVE ASSIGNMENT TO CORRECT STATE OF INCORPORATION IN THE ASSIGNMENT PREVIOUSLY RECORDED AT REEL 013287 FRAME 0638. Recorded Nov 19, 2004
From: QIAN, XUEJUN
To: KERR CORPORATION
Reel/Frame 015392/0830 →
RECORD TO CORRECT THE STATE OF INCORPORATION IN THE ASSIGNMENT DOCUMENT, PREVIOUSLY RECORDED AT REEL 013287 FRAME 0638. Recorded Nov 8, 2004
From: QIAN, XUEJUN
To: KERR CORPORAITON
Reel/Frame 015407/0127 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2002
From: QIAN, XUEJUN
To: KERR CORPORATION
Reel/Frame 013287/0638 →