IP Library Granted Patent US 11,739,223
Granted Patent B2
US 11,739,223 · App. 17/740,350 · Granted Aug 29, 2023

Surface primer compositions and methods of use

Inventors: Byung Jun Ahn (Goleta, CA); Bruce H. Lipshutz (Santa Barbara, CA); Sam L. Nguyen (Saratoga, CA)
Assignee: ENVISTA
C09D5/002A61K6/20A61K6/62A61K6/65A61K6/78B05D3/002B05D3/10B05D3/107C07C69/01C07C205/42C07C205/43C07C235/06C07C235/20C07C271/16C07D217/16C07F7/0896C07F9/12C07F9/62C09D7/63C08K5/107C08K5/13
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Quick Facts
Patent No.
US 11,739,223
App. No.
17/740,350
Granted
Aug 29, 2023
Kind
B2
Abstract

In one embodiment, the present application discloses a surface binding compound of the Formula I or Formula II: wherein the variables EG, EG1, SP1, SP2, SP3, Ar and BG are as defined herein. In another embodiment, the application discloses a method for forming a coating on a surface of a substrate using the surface binding compound of the Formula I or Formula II.

Claims (16)

1. A dental adhesive comprising a formulation or a mixture of:

a) the compounds of the Formula II:

wherein:

m is 1, 2 or 3; n is 1, 2 or 3; i is 1, 2 or 3;

each EG and EG1 is an end group independently selected from the group consisting of a C 1-12 alkyl, CH 2 ═CH—, CH 2 ═C(C 1-3 alkyl)-, CH 2 ═CHC(O)—, CH 2 ═C(C 1-3 alkyl)C(O)—, CH 2 ═CHC(O)O—, CH 2 ═C(C 1-3 alkyl)C(O)O—, and —Ar-(BG) a ; and wherein, a is 2 or 3; and wherein each BG is selected from the group consisting of —OH;

each of SP1, SP2 and SP3 is a spacer independently selected from the group consisting of —O—, —C(O)—, —C—, —CH—, —(CH 2 ) q —, —(CH(OH)) q —, —(CH 2 CH(OH)CH 2 ) q —, —(C(CH 3 ) 2 ) q —, —(CH(CH 3 )) q —, —OC(O)—, —CO 2 —, —OCH 2 CH 2 C(O)—, —C(O)CH 2 CH 2 C(O)—, —(CH 2 CH 2 O) p —, —(CH 2 CH 2 O) p CH 2 CH 2 —, —CH 2 CH 2 —(CH 2 CH 2 O) p —, —OCH(CH 2 O—) 2 —, wherein p is 1-6, and q is 1-6; and

b) a dental primer selected from the group consisting of phospho-SP-acrylates and phospho-SP-methacrylates.

2. The dental adhesive of claim 1 where the phospho-SP-methacrylates is 10-methacryloyloxydecyl dihydrogen phosphate.

3. The dental adhesive of claim 1 , further comprising a photoinitiator.

4. The dental adhesive of claim 3 , where photo-initiators are camphorquinone (CQ) and 2-dimethylaminoethyl methacrylate (DMAEMA).

5. The dental adhesive of claim 1 further comprising a solvent selected from the group consisting of acetone, alcohols and water, or mixtures thereof.

6. The dental adhesive of claim 1 further comprising a filler selected from the group consisting of mineral fillers, fumed silica, non-acid reactive fluoroaluminosilicate glasses fillers, quartz, ground glasses, ground polymer resins, non-water-soluble fluorides, silica gels, calcium silicate, zirconium silicate, zeolites and molecular sieves, or mixtures thereof.

7. The dental adhesive of claim 1 further comprising a dental adhesive selected from the group consisting of Bis-GMA, TEGDMA and DMAEMA.

8. The dental adhesive of claim 7 , wherein the adhesive provides wet adhesion and bonding durability without acid etching or self-etching.

9. The dental adhesive of claim 1 that is an orthodontic primer, adhesive, composite or a resin.

10. The dental adhesive of claim 1 , wherein the adhesive is a combination or a blend of a catechol methacrylate primer at 0.01-1 w/v % and a phosphomethacrylate primer at 0.1-30 w/v % in a solvent.

Continuity (6)
Division 16877058 · May 18, 2020
Division 15417825 · Jan 27, 2017
Provisional Application 62360677 · Jul 11, 2016
Provisional Application 62309156 · Mar 16, 2016
Provisional Application 62288195 · Jan 28, 2016
Related Publication 20230103027A1 · Mar 30, 2023