Dental materials and method of manufacture

Patent metadata

Field	Value
Publication number	US-9724276-B2
Application number	US-201314420036-A
Country	US
Kind code	B2
Filing date	Mar 15, 2013
Priority date	Aug 9, 2012
Publication date	Aug 8, 2017
Grant date	Aug 8, 2017

Abstract

Dental materials may be made from polyhydric phenols that are non-genotoxic and exhibit estrogenic activity less than that of bisphenol S, while exhibiting properties such as strength and flexibility comparable to those of conventional BPA-derived dental materials.

First claim

The invention claimed is:

1. A dental material comprising:
a free-radical polymerization initiator; and
a free-radically-polymerizable resin comprising:
a) at least two ethylenically unsaturated free-radically polymerizable end groups; and
b) a segment comprising:
(i) two or more aryl or heteroaryl groups in which each aryl or heteroaryl group includes an oxygen atom attached to the ring and (a) an ethyl, propyl, isopropyl, butyl, sec-butyl, or tert-butyl substituent group attached to the ring at an ortho or meta position relative to the oxygen atom, or (b) two substituent groups attached to the ring at both ortho positions relative to the oxygen atom;
(ii) and in which two or more aryl or heteroaryl groups are joined by an unsubstituted methylene bridge (—CH 2 —);

wherein the polymerizable resin is substantially free of polyhydric phenols having estrogenic activity greater than or equal to that of bisphenol S.

2. A dental material of claim 1 , wherein the at least two ethylenically unsaturated free-radically polymerizable end groups comprises one or more (meth)acrylate groups.

3. The dental material of claim 1 , wherein the segment has a structure of Formula I:

wherein:
H denotes a hydrogen atom, if present;
each R 1 is (a) an ethyl, propyl, isopropyl, butyl, sec-butyl, or tert-butyl substituent group attached to the ring at an ortho or meta position relative to the oxygen atom, or (b) independently an atom or group having an atomic weight of at least 15 Daltons attached to the ring at both ortho positions relative to the oxygen atom;
v is independently 2 to 4;
w is 4;
R 2 is a divalent unsubstituted methylene bridge (—CH 2 —);
n is 1;
t is 1;
two or more R 1 groups can join to form one or more cyclic groups, and
the polymerizable resin includes at least two free-radically polymerizable end groups.

4. The dental material of claim 3 , wherein the one or more R 1 groups independently comprise methyl groups.

5. The dental material of claim 3 , wherein each of the phenylene groups depicted in Formula I includes at least one R 1 group attached to the phenylene ring at an ortho position relative to the oxygen atom.

6. The dental material of claim 3 , wherein each of the phenylene groups depicted in Formula I includes two separate R 1 groups attached to the phenylene ring at both ortho positions relative to the oxygen atom.

7. The dental material of claim 3 , wherein the one or more R 1 groups independently comprise ethyl groups.

8. The dental material of claim 3 , wherein an R 1 group is attached to the phenylene ring at an ortho position relative to the oxygen atom, and a width measured perpendicular from a centerline of the phenylene ring to the maximal outside extent of the van der Waals volume of R 1 is greater than about 4.5 Angstroms.

9. The dental material of claim 3 , wherein the oxygen atom of each phenylene group depicted in Formula I is located at a para position relative to: R 2 .

10. The dental material of claim 1 , wherein the free-radically polymerizable resin is derived from one or more of the diglycidyl ether of 4,4′-methylenebis(2,6-di-t-butylphenol), the diglycidyl ether of 2,2′-methylenebis(4-methyl-6-t-butylphenol), the diglycidyl ether of 4,4′-methylenebis(2,6-dimethylphenol) or a derivative or combination thereof.

11. The dental material of claim 1 , wherein the dental material is a dental sealant, and further comprises a pigment.

12. The dental material of claim 1 , wherein the dental material is a dental composite or dental cement, and further comprises a filler.

13. The dental material of claim 12 , containing from about 10-90 wt % of the filler, from about 0.1 to about 5 wt % of the free-radical polymerization initiator and from about 5 to 95 wt % of the free-radically-polymerizable resin.

14. The dental material of claim 1 , wherein the segment of the polymerizable resin is derived from a polyhydric phenol or derivative thereof that exhibits a log Relative Proliferative Effect value in an MCF-7 cell proliferation assay less than that of bisphenol S.

15. A method of restoring a tooth comprising:
applying to the tooth a dental material comprising:
a free-radical polymerization initiator;
a filler; and
a free-radically-polymerizable resin comprising:
a) at least two ethylenically unsaturated free-radically polymerizable end groups; and
b) a segment comprising:
(i) two or more aryl or heteroaryl groups in which each aryl or heteroaryl group includes an oxygen atom attached to the ring and (a) an ethyl, propyl, isopropyl, butyl, sec-butyl, or tert-butyl substituent group attached to the ring at an ortho or meta position relative to the oxygen atom, or (b) two substituent groups attached in both ortho positions relative to the oxygen atom;
(ii) and in which two or more aryl or heteroaryl groups are joined by an unsubstituted methylene bridge (—CH 2 —);

wherein the polymerizable resin is substantially free of polyhydric phenols having estrogenic activity greater than or equal to that of bisphenol S; and

polymerizing the dental material to form a dental restoration.

16. A method for making a dental material, comprising mixing:
a) a free-radically-polymerizable resin comprising:
i) at least two ethylenically unsaturated free-radically polymerizable end groups and
ii) two or more aryl or heteroaryl ring segments having an oxygen atom attached to the ring and (a) an ethyl, propyl, isopropyl, butyl, sec-butyl, or tert-butyl substituent group attached to the ring at an ortho or meta position relative to the oxygen atom, or (b) two substituent groups attached in both ortho positions relative to the oxygen atom; and in which two or more aryl or heteroaryl ring segments are joined by an unsubstituted methylene bridge (—CH 2 —);
the resin being substantially free of polyhydric phenols having estrogenic activity greater than or equal to that of bisphenol S:

b) a polymerization initiator; and
c) optionally, a filler.

Assignees

• Valspar Sourcing Inc

Inventors

• Niederst Jeffrey
• Evans Richard H
• O'Brien Robert M
• Romagnoli Kevin
• Cavallin Carl
• Killilea T Howard
• Von Maier Mark S

Classifications

• A61P1/02

  Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis · CPC title

• A61K6/61 Primary

  Cationic, anionic or redox initiators · CPC title

• A61K6/887

  Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• A61K6/65

  Dyes · CPC title

• A61K6/083 Primary

  Human Necessities · mapped topic