IP Library Granted Patent US 11,904,031
Granted Patent B2
US 11,904,031 · App. 16/754,186 · Granted Feb 20, 2024

Orthodontic articles comprising polymerized composition comprising at least two free-radical initiators

Inventors: Saswata Chakraborty (Cottage Grove, MN); Benjamin C. MacMurray (St. Paul, MN); Eric W. Nelson (Stillwater, MN); Thomas P. Klun (Lakeland, MN); Richard J. Pokorny (Maplewood, MN); Wayne S. Mahoney (St. Paul, MN); Chad M. Amb (Roberts, WI); George W. Griesgraber (Eagan, MN); Dana R. Reed (Minneapolis, MN); Ahmed S. Abuelyaman (Woodbury, MN); Robert S. Clough (St. Paul, MN); James D. Hansen (White Bear Lake, MN); Daniel J. Skamser (Ham Lake, MN); Ian Dailey (Maplewood, MN); John M. Riedesel (San Jose, CA)
Assignee: 3M Innovative Properties Company
A61K6/62A61C7/002A61C7/08A61K6/893B29C64/124B33Y10/00B33Y70/00B33Y80/00C08L75/14
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Quick Facts
Patent No.
US 11,904,031
App. No.
16/754,186
Granted
Feb 20, 2024
Kind
B2
Abstract

An orthodontic article is described comprising the reaction product of a free-radically polymerizable resin; a first free-radical photoinitiator having sufficient absorbance at a first wavelength range; and a second free-radical initiator selected from a second photoinitiator having sufficient absorbance at a second wavelength range, wherein the second wavelength range is different than the first wavelength range, or a thermal free-radical initiator. In some embodiments, the first free-radical photoinitiator exhibits a maximum absorbance at a wavelength of the range of 370-380 nm or 320-330 nm and/or comprises photoinitiator groups selected from acyl phosphine oxide or alkyl amine acetophenone. Also described are photopolymerizable compositions and methods.

Claims (23)

1. An orthodontic article comprising a cured composition comprising

a free-radically polymerizable resin comprising a urethane (meth)acrylate comprising polymerized units derived from a diol selected from polycarbonate diol or polyester diol;

a first free-radical photoinitiator having sufficient absorbance at a first wavelength range; and

a second free-radical initiator selected from a second photoinitiator having sufficient absorbance at a second wavelength range, wherein the second wavelength range is different than the first wavelength range, or a thermal free-radical initiator.

2. The orthodontic article of claim 1 wherein a 1 g/liter acetonitrile solution of the first free-radical photoinitiator, at a pathlength of 1 cm, has an absorbance of greater than 0.01 at a wavelength of 385 nm when measured with a spectrophotometer.

3. The orthodontic article of claim 1 wherein a 1 g/liter acetonitrile solution of the first free-radical photoinitiator, at a pathlength, of 1 cm has an absorbance of greater than 0.2 for a 1 g/liter solution of the first free-radical photoinitiator in acetonitrile at a wavelength of 385 nm when measured with a spectrophotometer.

4. The orthodontic article of claim 1 wherein the first free-radical photoinitiator has a maximum absorbance at a wavelength of the range of 370-380 nm or 320-330 nm.

5. The orthodontic article of claim 1 wherein the first free-radical photoinitiator comprises photoinitiator groups selected from acyl phosphine oxide or alkyl amine acetophenone.

6. The orthodontic article of claim 1 wherein the second free-radical initiator is a thermal initiator.

7. The orthodontic article of claim 1 wherein a 1 g/liter acetonitrile solution of the second photoinitiator, at a pathlength of 1 cm, has an absorbance of greater than 0.01 at a wavelength of 365 nm when measured with a spectrophotometer.

8. The orthodontic article of claim 1 wherein the second photoinitiator has a maximum absorbance at a wavelength of the range 325-330 nm.

9. The orthodontic article of claim 1 wherein the second photoinitiator comprises photoinitiator groups selected from benzil ketal or hydroxy-acetophenone.

10. The orthodontic article of claim 1 wherein a 1 g/liter acetonitrile solution of the second photoinitiator, at a pathlength of 1 cm, has an absorbance of less than 0.1 at a wavelength of 365 nm.

11. The orthodontic article of claim 1 wherein the composition comprises 0.1 to 5 wt. % of photoinitiators based on the total weight of the polymerizable composition.

12. The orthodontic article of claim 1 wherein the polymerizable composition further comprises an ultraviolet absorber.

13. The orthodontic article of claim 1 wherein the free-radically polymerizable resin comprises 25 to 70 wt. % of at least one monofunctional reactive diluent.

14. The orthodontic article of claim 13 wherein the monofunctional reactive diluent comprises at least one monofunctional reactive diluent having a T g of 25 degrees Celsius or greater.

15. The orthodontic article of claim 13 wherein the monofunctional reactive diluent comprises at least one monofunctional reactive diluent where a homopolymer thereof has a T g of 60 degrees Celsius or greater.

16. The orthodontic article of claim 13 wherein the monofunctional reactive diluent comprises at least one monofunctional reactive diluent having a log P value of greater than 1.5.

17. The orthodontic article of claim 13 wherein the orthodontic article comprises less than 0.1 wt.-% extractables in a solution of 5% ethanol in water.

18. The orthodontic article of claim 1 wherein the cured composition exhibits an elongation at break of 15% or greater and a tensile strength at yield of at least 10 MPa as determined according to ASTM D638-14 after conditioning in phosphate-buffered saline having a pH of 7.4 for 24 hours at a temperature of 37° C.

19. The orthodontic article of claim 1 wherein the cured composition polymerized composition exhibits a 3-point bend modulus of at least 100 MPa as determined according to dynamic mechanical analysis at 2% strain after conditioning in deionized water at 20-25° C. for 48 hours.

20. The orthodontic article of claim 1 wherein the orthodontic article is orthodontic tray aligner article.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066431/0915 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2020
From: CHAKRABORTY, SASWATA; MAC MURRAY, BENJAMIN C.; NELSON, ERIC W.; KLUN, THOMAS P.; POKORNY, RICHARD J.; MAHONEY, WAYNE S.; AMB, CHAD M.; GRIESGRABER, GEORGE W.; REED, DANA R.; ABUELYAMAN, AHMED S.; CLOUGH, ROBERT S.; HANSEN, JAMES D.; SKAMSER, DANIEL J.; DAILEY, IAN; RIEDESEL, JOHN M.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 052329/0497 →