Low viscosity photo-curable resins for the direct fabrication of orthodontic appliances

Patent metadata

Field	Value
Publication number	US-12351660-B2
Application number	US-202318529570-A
Country	US
Kind code	B2
Filing date	Dec 5, 2023
Priority date	Mar 2, 2020
Publication date	Jul 8, 2025
Grant date	Jul 8, 2025

Abstract

This disclosure provides low-viscosity resins for producing polymers with properties suitable for use in various mechanical appliances, such as orthodontic appliances (e.g., aligners). The low-viscosity resins may be photo-curable and can be used with direct fabrication methods and equipment. In various embodiments, the polymeric materials produced from the low-viscosity resins described herein have high toughness while remaining resistant to stress relaxation. Low-viscosity, photo-curable resins described herein have reduced hydrogen bonding in comparison to traditional materials (e.g., materials having high urethane content) used in orthodontic appliances.

First claim

What is claimed is:

1. A method of forming an object comprising a polymeric material by additive manufacturing, the method comprising:
providing a photo-curable resin, the photo-curable resin comprising:
an oligomer having a number-average molecular weight of greater than 3,000 Da; and
an initiator,
wherein the photo-curable resin comprises less than 8 wt % hydrogen bonding units and has a viscosity less than or equal to 15,000 cP at 25° C.;

curing the photo-curable resin, thereby forming the polymeric material; and
fabricating the object with the polymeric material.

2. The method of claim 1 , wherein the polymeric material is characterized by one or more of:
a tensile modulus greater than or equal to 200 MPa;
a flexural stress of greater than or equal to 1.5 MPa remaining after 24 hours in a wet environment at 37° C.;
a hardness from 60 Shore A to 85 Shore D; and
an elongation at break greater than or equal to 15%.

3. The method of claim 1 , wherein the polymeric material has greater than 60% conversion of double bonds to single bonds, as measured by FTIR.

4. The method of claim 1 , wherein the polymeric material has less than 5 wt % extractable materials.

5. The method of claim 1 , wherein the polymeric material is characterized by a water uptake of less than 25 wt %, less than 20 wt %, less than 15 wt %, less than 10 wt %, less than 5 wt %, less than 4 wt %, less than 3 wt %, less than 2 wt %, less than 1 wt %, less than 0.5 wt %, less than 0.25 wt %, or less than 0.1 wt %.

6. The method of claim 1 , wherein curing the photo-curable resin comprises exposing the photo-curable resin to a light source.

7. The method of claim 1 , further comprising heating the polymeric material to an elevated temperature.

8. The method of claim 7 , wherein the elevated temperature is from 40° C. to 150° C.

9. The method of claim 7 , wherein heating the polymeric material to the elevated temperature occurs after curing the photo-curable resin.

10. The method of claim 1 , wherein fabricating the object with the polymeric material comprises printing with a 3D printer.

11. The method of claim 1 , wherein fabricating the object with the polymeric material comprises digital light projection.

12. The method of claim 1 , wherein fabricating the object with the polymeric material comprises high temperature lithography.

13. The method of claim 1 , wherein the object is an orthodontic appliance.

14. The method of claim 13 , wherein the orthodontic appliance is an aligner, expander or spacer.

15. The method of claim 13 , wherein the orthodontic appliance comprises a plurality of tooth receiving cavities configured to reposition teeth from a first configuration toward a second configuration.

16. The method of claim 13 , wherein the orthodontic appliance is one of a plurality of orthodontic appliances configured to reposition the teeth from an initial configuration toward a target configuration.

17. The method of claim 13 , wherein the orthodontic appliance is one of a plurality of orthodontic appliances configured to reposition the teeth from an initial configuration toward a target configuration according to a treatment plan.

18. The method of claim 12 , wherein the high temperature lithography comprises applying heating to the photo-curable resin to temperatures between 90° C. and 120° C.

19. The method of claim 1 , wherein the viscosity of the photo-curable resin is less than 1,000 cP at 110° C.

20. The method of claim 1 , wherein the initiator comprises a photoinitiator.

21. The method of claim 1 , wherein the initiator comprises a thermal initiator.

22. The method of claim 1 , wherein the oligomer comprises an aliphatic urethane (meth)acrylate, a polybutadiene urethane (meth)acrylate or a polyester urethane (meth)acryalte.

23. The method of claim 1 , wherein the oligomer comprises two or more functional groups.

24. The method of claim 23 , wherein the functional groups comprise an acrylate, a methacrylate, an acrylamide, a vinyl group, a vinyl ether, a vinyl ester, a thiol, an allyl ether, a norbornene, a vinyl acetate, a maleate, a fumarate, a maleimide, an epoxide, a ring-strained cyclic ether, a ring-strained thioether, a cyclic ester, a cyclic carbonate, a cyclic silane, a cyclic siloxane, a hydroxyl, an amine, an isocyanate, a blocked isocyanate, an acid chloride, an activated ester, a Diels-Alder reactive group, a furan, a cyclopentadiene, an anhydride, an anthracene, an acenaphthalene, a coumarone, a Norrish Type 1 or 2 material, an azide or a combination thereof.

25. The method of claim 1 , further comprising a reactive diluent.

26. The method of claim 25 , wherein the reactive diluent comprises a (poly)glycol di(meth)acrylate, a triethylene glycol di(meth)acrylate, a tetraethylene glycol di(meth)acrylate, bisphenol A di(meth) acrylate, a hydrogenated form of bisphenol A di(meth)acrylate, a methacrylate-or acrylate-terminated polyester oligomer, 4,4′-isopropylidenedicyclohexanol di(meth)acrylate, a salicylic ester (meth)acrylate, or cycloalkyl salicylate (meth)acrylate.

27. The method of claim 1 , wherein the photo-curable resin further comprises one or more of: a crosslinking modifier, a light blocker, a solvent, and a glass transition temperature modifier.

Assignees

• Align Technology Inc

Inventors

• Carter Blaine
• Chavez Jennifer
• Pickens Lance Robert
• Cole Michael Christopher
• Dorfinger Peter
• Chen Yan

Classifications

• A61L27/16

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

• A61L27/14

  Macromolecular materials · CPC title

• C08K5/14

  Peroxides · CPC title

• C08F20/34

  Esters containing nitrogen {, e.g. N,N-dimethylaminoethyl (meth)acrylate} · CPC title

• B29C2071/0027

  Removing undesirable residual components, e.g. solvents, unreacted monomers · CPC title