IP Library Granted Patent US 12,351,668
Granted Patent B2
US 12,351,668 · App. 17/605,289 · Granted Jul 8, 2025

Orthodontic articles comprising polymerized composition with pendent cyclic moieties, methods, and polymerizable compositions

Inventors: Thomas P. Klun (Lakeland, MN); Chad M. Amb (Roberts, WI); Richard J. Pokorny (Maplewood, MN); Saswata Chakraborty (Cottage Grove, MN); Benjamin C. Mac Murray (Minneapolis, MN); Tianyu Wu (St. Paul, MN); Ahmed S. Abuelyaman (Woodbury, MN); Yongshang Lu (Woodbury, MN); Daniel J. Skamser (Ham Lake, MN); Karl J. L. Geisler (St. Paul, MN); John M. Riedesel (San Jose, CA)
Assignee: Solventum Intellectual Properties Company
C08F290/067A61C7/08B29C64/124B33Y10/00B33Y70/00B33Y80/00B29K2105/0002B29L2031/753
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Quick Facts
Patent No.
US 12,351,668
App. No.
17/605,289
Granted
Jul 8, 2025
Kind
B2
Abstract

Polymerizable compositions suitable for use for 3D printed (e.g. orthodontic) articles, especially orthodontic alignment trays, are described. The polymerizable composition comprises a) 30-70 parts by weight of (meth)acrylate monomer(s); and b) urethane (meth)acrylate polymer; wherein the reaction product comprises at least 1 wt. % polymerized units of a multifunctional compound comprising pendent cyclic moieties. The orthodontic article comprises the reaction product of a polymerizable composition as described herein. The urethane (meth)acrylate polymer typically comprises polymerized units of a multifunctional compound comprising pendent cyclic moieties and/or at least one (meth)acrylate monomer comprises polymerized units of a multifunctional compound comprising pendent cyclic moieties. Also described are methods of making an article, non-transitory machine-readable medium comprising data representing a three-dimensional model of an article, and systems.

Claims (38)

1. An orthodontic article comprising a reaction product of a polymerizable composition comprising:

a) 30-70 parts by weight of (meth)acrylate monomer(s); and

b) a urethane (meth)acrylate polymer comprising a reaction product of at least: a diol lacking pendent cyclic moieties, a polyisocyanate, and a reactive compound comprising pendent cyclic moieties;

wherein the reaction product comprises at least 1 weight percent polymerized units of a multifunctional compound comprising pendent cyclic moieties.

2. The orthodontic article of claim 1 , wherein the pendent cyclic moieties are derived from an isocyanate reactive compound or a hydroxyl reactive compound comprising pendent cyclic moieties.

3. The orthodontic article of claim 1 , wherein the urethane (meth)acrylate polymer comprises a reaction product of:

i) an isocyanate reactive or a hydroxyl reactive compound comprising a pendent cyclic moiety,

ii) a polyol lacking pendent cyclic moieties,

iii) a diisocyanate lacking pendent cyclic moieties, and

iv) a hydroxy functional (meth)acrylate or an isocyanate functional (meth)acrylate.

4. The orthodontic article of claim 3 , wherein the urethane (meth)acrylate polymer further comprises a reaction product of a diol (meth)acrylate.

5. The orthodontic article of claim 3 , wherein the diol lacking pendent cyclic moieties is at least one of: a polyester diol, a polycarbonate diol, or a polyether diol.

6. The orthodontic article of claim 1 , wherein at least one of the (meth)acrylate monomer(s) comprises at least one pendent cyclic moiety.

7. The orthodontic article of claim 1 , wherein the urethane (meth)acrylate polymer and the (meth)acrylate monomer(s) are present at a weight ratio ranging from 2:1 to 1:2.

8. The orthodontic article of claim 1 , wherein the (meth)acrylate monomer(s) comprise at least one monofunctional (meth)acrylate monomer.

9. The orthodontic article of claim 6 , wherein the (meth)acrylate monomer has a log P value of greater than 1, 1.5, 2, 2.5, or 3.

10. The orthodontic article of claim 6 , wherein the (meth)acrylate monomer has a glass transition temperature of at least 30° C., 40° C., 50° C., 60° C., 70° C., 80° C., or 90° C.

11. The orthodontic article of claim 1 , wherein the urethane (meth)acrylate polymer comprises the formula:

(A) p -Q-OC(═O)NH—R di —NHC(═O)O-Q-(A) p ,

wherein A has the formula —OC(═O)C(R 1 )═CH 2 , wherein R 1 is H or an alkyl of 1 to 4 carbon atoms, p is 1 or 2, Q is a polyvalent organic linking group, and R di is the residue of a diisocyanate.

12. The orthodontic article of claim 1 , wherein the polymerizable composition is polymerized and exhibits;

an elongation at break of 15% or greater and a tensile strength at yield of at least 10 megapascals (MPa) as determined according to ASTM D638-14 after conditioning in phosphate-buffered saline with a pH of 7.4 for 24 hours at 37° C., or

a loss of relaxation modulus of less than 70%, 65%, 60%, 55%, or 50%, as determined according to Dynamic Mechanical Analysis after conditioning in deionized water for 48 hours at 22-25° C.

13. The orthodontic article of claim 1 , wherein the polymerizable composition is polymerized and exhibits a loss of relaxation modulus of less than 70%, 65%, 60%, 55%, or 50%, as determined according to Dynamic Mechanical Analysis after conditioning in deionized water for 48 hours at 22-25° C.

14. The orthodontic article of claim 1 , wherein the polymerizable composition comprises a photoinitiator.

15. The orthodontic article of claim 1 , wherein the orthodontic article is an orthodontic alignment tray.

16. A polymerizable composition comprising:

a) 30-70 parts by weight of (meth)acrylate monomer(s); and

b) a urethane (meth)acrylate polymer comprising a reaction product of at least: a diol lacking pendent cyclic moieties, a polyisocyanate, and a reactive compound comprising pendent cyclic moieties;

wherein a reaction product of the polymerizable composition comprises at least 1 weight percent polymerized units of a multifunctional compound comprising the pendent cyclic moieties.

17. A method of making an article comprising:

a) providing a photopolymerizable composition according to claim 16 ;

b) selectively curing the photopolymerizable composition to form the article; and

c) repeating steps a) and b) to form multiple layers and create the article comprising a three-dimensional structure.

18. A method comprising:

a) receiving, by a manufacturing device having one or more processors, a digital object comprising data specifying a plurality of layers of an article; and

b) generating, with the manufacturing device by an additive manufacturing process, the article based on the digital object, the article comprising a reaction product of a photopolymerizable composition according to claim 16 .

19. The orthodontic article of claim 11 , wherein Q comprises a straight or branched chain or cycle-containing aliphatic connecting group.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066443/0600 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2021
From: KLUN, THOMAS P.; AMB, CHAD M.; POKORNY, RICHARD J.; CHAKRABORTY, SASWATA; MAC MURRAY, BENJAMIN C.; WU, TIANYU; ABUELYAMAN, AHMED S.; LU, YONGSHANG; SKAMSER, DANIEL J.; GEISLER, KARL J.L.; RIEDESEL, JOHN M.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 057861/0016 →
Continuity (2)
Provisional Application 62850721 · May 21, 2019
Related Publication 20220242991A1 · Aug 4, 2022
References Cited (82)
US 3429722A · Economy · 1969 [cited by applicant]
US 3795524A · Sowman · 1974 [cited by applicant]
US 4047965A · Karst · 1977 [cited by applicant]
US 4591626A · Kawai · 1986 [cited by applicant]
US 4954462A · Wood · 1990 [cited by applicant]
US 5109097A · Klun · 1992 [cited by examiner]
US 5130347A · Mitra · 1992 [cited by applicant]
US 5185299A · Wood · 1993 [cited by applicant]
US 5780154A · Okano · 1998 [cited by applicant]
US 5981621A · Clark · 1999 [cited by applicant]
US 6183593B1 · Narang · 2001 [cited by applicant]
US 6200732B1 · Tamura · 2001 [cited by applicant]
US 7622535B2 · Dairoku · 2009 [cited by applicant]
US 8853338B2 · Wang · 2014 [cited by applicant]
US 9012531B2 · Abuelyaman · 2015 [cited by applicant]
US 9205601B2 · DeSimone · 2015 [cited by applicant]
US 9295617B2 · Eckert · 2016 [cited by applicant]
US 9360757B2 · DeSimone · 2016 [cited by applicant]
US 9463144B2 · Shukla · 2016 [cited by applicant]
US 20050090575A1 · Chaput · 2005 [cited by applicant]
US 20070031791A1 · Cinader, Jr. · 2007 [cited by applicant]
US 20080248442A1 · Raby · 2008 [cited by applicant]
US 20090054543A1 · Nozawa · 2009 [cited by examiner]
US 20110091832A1 · Kim · 2011 [cited by applicant]
US 20110183298A1 · Sun · 2011 [cited by applicant]
US 20130095446A1 · Andreiko · 2013 [cited by applicant]
US 20130130203A1 · Velamakanni · 2013 [cited by applicant]
US 20140356799A1 · Cinader, Jr. · 2014 [cited by applicant]
US 20150044623A1 · Rundlett · 2015 [cited by applicant]
US 20160081887A1 · Abuelyaman · 2016 [cited by examiner]
US 20160288479A1 · Shuey · 2016 [cited by applicant]
US 20170007362A1 · Chen · 2017 [cited by applicant]
US 20170151718A1 · Rolland · 2017 [cited by applicant]
US 20190083208A1 · Hansen · 2019 [cited by applicant]
CA 3008362 · 2017 [cited by applicant]
CN 106029046A · 2016 [cited by applicant]
JP 2002161124 · 2002 [cited by applicant]
WO WO199615179 · 1996 [cited by applicant]
WO WO2009045752 · 2009 [cited by applicant]
WO 2012003136A1 · 2012 [cited by applicant]
WO WO2015094842 · 2015 [cited by applicant]
WO WO2015126666 · 2015 [cited by applicant]
WO WO2015126666A1 · 2015 [cited by examiner]
WO WO2016094272 · 2016 [cited by applicant]
WO WO2016109660 · 2016 [cited by applicant]
WO WO2016148960 · 2016 [cited by applicant]
WO WO2016149007 · 2016 [cited by applicant]
WO WO2018005501 · 2018 [cited by applicant]
WO WO2018106531 · 2018 [cited by applicant]
WO WO2018119026 · 2018 [cited by applicant]
WO WO2019023009 · 2019 [cited by applicant]
WO WO2019023120 · 2019 [cited by applicant]
WO WO2019023166 · 2019 [cited by applicant]
WO WO2019048963 · 2019 [cited by applicant]
WO WO2019103855 · 2019 [cited by applicant]
WO WO2019104072 · 2019 [cited by applicant]
WO WO2019104079 · 2019 [cited by applicant]
WO WO2019175716 · 2019 [cited by applicant]
WO WO2019224699 · 2019 [cited by applicant]
WO WO2019244007 · 2019 [cited by applicant]
WO 2020003197A2 · 2020 [cited by applicant]
WO WO2020003169 · 2020 [cited by applicant]
WO WO2020005411 · 2020 [cited by applicant]
WO WO2020005413 · 2020 [cited by applicant]
WO WO2020104873 · 2020 [cited by applicant]
Ali, “Relationship Between Physical-Mechanical Properties and Glass Transition Temperatures of UV-Cured Polymers”, Polymer-Plastics Technology and Engineering, May 1998, vol. 37, No. 2, pp. 175-189, XP055553669. [cited by applicant]
Bishop, “Multiple Photoinitiators for Improved Performance”, Proceedings of the Radtech NA Conference Proceedings, Jan. 1, 2008, 8 pages, XP055558707. [cited by applicant]
Chun, “Preparation and Characterization of UV Cured Optical Films Containing a Fluorene Compound”, Molecular Crystals and Liquid Crystals, 2015, vol. 622, No. 1, pp. 6-13. [cited by applicant]
Elles, “De Quelques Polyacrylamides”, 1959, Chimie Moderne, vol. 4, No. 26, pp. 53-57. [cited by applicant]
Fang, “The influence of monobutyl itaconate and β-carboxyethyl acrylate on acrylic latex pressure sensitive adhesives”, International Journal of Adhesion and Adhesives, May 2018, vol. 84, pp. 387-393. [cited by applicant]
Fleischhaker, “Glass-Transition-, Melting-, and Decomposition Temperatures of Tailored Polyacrylates and Polymethacrylates: General Trends and Structure-Property Relationships”, Macromolecular Chemistry and Physics, 201… [cited by applicant]
Hopfinger, “Molecular Modeling of Polymers. IV. Estimation of Glass Transition Temperatures”, Journal of Polymer Science: Part B: Polymer Physics, 1988, vol. 26, pp. 2007-2028. [cited by applicant]
Jakubowski, “Comparison of thermomechanical properties of statistical, gradient and block copolymers of isobornyl acrylate and n-butyl acrylate with various acrylate homopolymers”, Polymer, 2008, vol. 49, pp. 1567-1578. [cited by applicant]
Matsumoto, “Radical Polymerization of 4-tert-Butylcyclohexyl Methacrylate: Polymerization Kinetics and Polymer Properties”, Macromolecules 1993, vol. 26, No. 7, pp. 1659-1685. [cited by applicant]
Matsumoto, “Synthesis and Characterization of Poly(I-adamantyl methacrylate): Effects of the Adamantyl Group on Radical Polymerization Kinetics and Thermal Properties of the Polymer”, Macromolecules 1991, vol. 24, No. 1… [cited by applicant]
Matsumoto, “Synthesis and Thermal Properties of Poly(cycloalkyl methacrylate)s Bearing Bridged- and Fused-Ring Structures”, Journal of Polymer Science: Part A: Polymer Chemistry, 1993, vol. 31, pp. 2531-2539. [cited by applicant]
Methacrylate Resins, E.I. du Pont de Nemours & Co., Industrial and Engineering Chemistry, Oct. 1936, vol. 28, No. 10, pp. 1160-1163. [cited by applicant]
Russell, “Thermal and Dynamic Mechanical Relaxation Behavior of Stereoregular Poly(2-Hydroxyethyl Methacrylate)”, Journal of Polymer Science: Polymer Physics, 1980, vol. 18, pp. 1271-1283. [cited by applicant]
Song, “In Vitro Evaluation of Chemically Cross-Linked Shape-Memory Acrylate-Methacrylate Copolymer Networks as Ocular Implants”, Journal of Physical Chemistry B, 2010, vol. 114, No. 21, pp. 7172-7178. [cited by applicant]
Turner, “The glass transition temperature of poly(N-vinyl pyrrolidone) by differential scanning calorimetry”, Polymer, May 1985, vol. 26, pp. 757-762. [cited by applicant]
Wilson, “Thermal Expansion of Amorphous Polymers at Atmospheric Pressure. I. Experimental”, Macromolecules, 1973, vol. 6, No. 6, pp. 902-908. [cited by applicant]
International Search Report for PCT International Application No. PCT/IB2020/054745, mailed on Aug. 27, 2020, 5 pages. [cited by applicant]