Dental impression material

Patent metadata

Field	Value
Publication number	US-11925697-B2
Application number	US-201916982094-A
Country	US
Kind code	B2
Filing date	Mar 7, 2019
Priority date	Mar 7, 2018
Publication date	Mar 12, 2024
Grant date	Mar 12, 2024

Abstract

A photocurable dental impression material comprising:
(a) a mixture of polymerizable silicone compounds each having two or more polymerizable (meth)acrylate groups, said mixture having a dynamic viscosity at 25° C. of from 1 to 100 Pas; (b) a filler; (c) a photo initiator system, wherein the mixture of polymerizable silicone compounds comprises based on the total weight of the mixture of polymerizable silicone compounds
(a) 10 to 90 percent by weight of high-molecular polymerizable silicone compounds having a molecular weight in the range of from more than 4000 up to 10.000; and (b) 90 to 10 percent by weight of polymerizable silicone compounds having a molecular weight in the range of from 300 to 4000.

First claim

The invention claimed is:

1. A photocurable dental impression material comprising:
(a) a mixture of polymerizable silicone compounds each having two or more polymerizable (meth)acrylate groups, said mixture having a dynamic viscosity at 25° C. of from 1 to 100 Pas;
(b) a filler;
(c) a photo initiator system,
wherein the mixture of polymerizable silicone compounds comprises based on the total weight of the mixture of polymerizable silicone compounds
(i) 10 to 90 percent by weight of high-molecular polymerizable silicone compounds having a molecular weight in the range of from more than 4000 up to 10,000; and
(ii) 90 to 10 percent by weight of polymerizable silicone compounds having a molecular weight in the range of from 300 to 4000,

wherein a ratio of (meth)acrylate groups per total molecular weight of the polymerizable silicone compounds of (ii) is higher than a ratio of (meth)acrylate groups per total molecular weight of molecules of the high-molecular weight polymerizable silicone compounds of (i).

2. The photocurable dental impression material according to claim 1 , which further comprises up to 20 percent by weight based on the total weight of the composition of polymerizable (meth)acrylates or (meth)acrylamides.

3. The photocurable dental impression material according to claim 1 , wherein the polymerizable silicone compounds are compounds of the following formula (I):

wherein
R 1 represents a (meth)acrylate group containing organic residue, a C 1-4 alkyl group, a group of the formula [—OSiR′ 2 ] n R′, or two groups R 1 or a group R 1 and R 2 form together a group [—OSiR′ 2 ] n —, wherein the R′, which may be the same or different, independently represent a C 1-4 alkyl group or an (meth)acrylate group containing organic residue and n is an integer of from 1 to 20;
R 2 represents a C 1-4 alkyl group or a group of the formula [—OSiR″ 2 ] m R″, or two groups R 2 or a group R 1 and R 2 form together a group [—OSiR″ 2 ] m —, wherein the R″, which may be the same or different, independently represent a C 1-4 alkyl group and m is an integer of from 1 to 20;
L represents a divalent C 1-20 organic linker group;
a represents 0 or an integer of from 1 to 20;
b represents 0 or an integer of from 1 to 20;
c represents 0 or an integer of from 1 to 20;
d represents 0 or an integer of from 1 to 20;
provided that at least two (meth)acrylate groups are present in the compound of formula (I).

4. The photocurable dental impression material according to claim 3 , wherein R 1 is a group of the following formula (II)

wherein
R represents a hydrogen atom or a methyl group; and
x is 0 or an integer of from 1 to 8.

5. The photocurable dental impression material according to claim 1 , wherein the mixture of polymerizable silicone compounds each having two or more polymerizable (meth)acrylate groups comprises 1,3-Bis(3-methacryloxypropyl)tetramethyldisiloxane (BMTMDS), 1,3-bis(3-methacyloxypropyl)tetrakis(trimethylsiloxy)disiloxane, methacryloxypropyl terminated polydimethylsiloxane, a difunctional aliphatic silicone acrylate, and/or a hexafunctional silicone urethane acrylate.

6. The photocurable dental impression material according to claim 1 , wherein the photo initiator comprises a sensitizer having an absorption maximum in the range of from 400 to 800 nm.

7. The curable dental impression material according to claim 1 , wherein the photo initiator further comprises:
(1) an iodonium compound of the following formula (III):
R 7 —I + —R 8 A −   (VII)

wherein
R 7 and R 8
which are independent from each other, represent an organic moiety, and
A − is an anion;

(2) a sulfonium compound of the following formula (IV):
R 9 R 10 R 11 S + A −   (IV)

wherein
R 9 , R 10 and R 11
which are independent from each other, represent an organic moiety or wherein any two of R 9 , R 10 and R 11 form a cyclic structure together with the sulfur atom to which they are bound, and
A − is an anion; and/or

(3) a phosphonium compound of the following formula (V):
R 12 R 13 R 14 R 15 P + A −   (V)

wherein
R 12 , R 13 , R 14 , and R 15
which are independent from each other, represent an organic moiety, and

A − is an anion.

8. The photocurable dental impression material according to claim 1 , which comprises 40 to 90 percent by weight based on the total weight of the dental impression material of mixture of polymerizable silicone compounds each having two or more polymerizable (meth)acrylate groups.

9. The photocurable dental impression material according to claim 1 , which comprises 10 to 60 percent by weight based on the total weight of the dental impression material of a filler.

10. The curable dental impression material according to claim 1 , wherein the filler has a mean particle size in the range of from 0.05 to 5 μm.

11. The curable dental impression material according to claim 1 , wherein the curable dental impression material is a one-pack composition packaged in a syringe or provided on a ready-to-use dental impression tray.

12. The photocurable dental impression material according to claim 1 , wherein the mixture of polymerizable silicone compounds has a dynamic viscosity at 25° C. of from 5 to 80 Pas.

13. The photocurable dental impression material according to claim 12 , wherein the mixture of polymerizable silicone compounds has a dynamic viscosity at 25° C. of from 10 to 70 Pas.

14. The photocurable dental impression material according to claim 1 , wherein the mixture of polymerizable silicone compounds comprises based on the total weight of the mixture of polymerizable silicone compounds
(i) 50 to 85 percent by weight of polymerizable silicone compounds having a molecular weight in the range of from more than 4000 up to 10,000; and
(ii) 15 to 50 percent by weight of polymerizable silicone compounds having a molecular weight in the range of from 300 to 4000.

15. The photocurable dental impression material according to claim 1 , wherein the polymerizable silicone compounds of paragraph (i) comprise either or both of 1,3-bis(3-methacryloxypropyl)tetramethyldisiloxane (BMTMDS) and 1,3-bis(3-methacyloxypropyl)tetrakis(trimethylsiloxy)disiloxane.

16. The photocurable dental impression material according to claim 1 , wherein the polymerizable silicone compounds of paragraph (ii) comprise a difunctional aliphatic silicone acrylate.

17. The photocurable dental impression material according to claim 1 , wherein the photo initiator comprises camphorquinone or tert-butyl(tert-butyldimethylsilyl)glyoxylate.

18. A method for preparing a dental impression, which method comprises
(a) providing a curable dental impression material according to claim 1 ;
(b) taking an impression of a dental structure; and
(c) curing the dental impression material with light having a wavelength in the range of 200 to 800 nm.

Assignees

• Dentsply Detrey Gmbh
• Dentsply Sirona Inc

Inventors

• Klee Joachim
• Szillat Florian
• Maier Maximilian
• Yon Marjorie
• Lalevée Jacques
• Kirschner Julie
• Morlet-Savary Fabrice
• Dietlin Céline

Classifications

• A61K6/90 Primary

  Compositions for taking dental impressions · CPC title

• A61C19/003

  Apparatus for curing resins by radiation · CPC title

• A61C9/0006

  Impression trays · CPC title

• A61K6/896 Primary

  Polyorganosilicon compounds · CPC title