Methods for making biocompatible polymerizable acrylate products
View Patent ↗Sugar-acrylic monomers are synthesized to have a carbohydrate moiety linked to an acrylate group. The sugar-acrylic monomers may be polymerized to form polymers, adhesives, hydrogels, and the like. The sugar-acrylic monomers and polymers may be used in tissue engineering, adhesives and sealers, wound healing, and the like.
1. A method for making a biocompatible polymerizable acrylate product, the method comprising:
providing a carbohydrate having a plurality of hydroxyl groups;
contacting the carbohydrate with a protecting group agent to yield a protected carbohydrate;
linking a polymerizable acrylate group to the protected carbohydrate to yield a polymerizable acrylate monomer having a pendant carbohydrate moiety, wherein the step of linking the polymerizable acrylate group to the protected carbohydrate includes bonding a cyanoacrylate intermediate group to the protected carbohydrate and then converting the cyanoacrylate intermediate group to a polymerizable cyanoacrylate; and
placing the polymerizable acrylate monomer in a water-tight sealed packaging, the sealed packaging being configured to have the seal broken when it is desired to use the polymerizable acrylate monomer.
2. The method of claim 1 , wherein providing the carbohydrate comprises providing a hexose, a pentose, a derivative thereof, or a combination thereof.
3. The method of claim 1 , wherein providing the carbohydrate comprises providing a monosaccharide selected from the group consisting of allose, altrose, glucose, mannose, gulose, idose, galactose, talose, psicose, fructose, sorbose, tagatose, ribose, arabinose, xylose, lyxose, ribulose, xylulose, erythose, threose, erythrulose, glyceraldehydes, altro-heptulose, L-glycero-D-manno-heptose, derivatives thereof, and combinations thereof.
4. The method of claim 1 , wherein the bonding of the cyanoacrylate intermediate group to the protected carbohydrate comprises:
contacting the protected carbohydrate with an acid halide to yield a beta halide protected carbohydrate;
contacting the beta halide protected carbohydrate with a cyanoacetate to yield a cyanoacrylate intermediate; and
condensing the cyanoacrylate to yield a cyanoacrylate oligomer; and
cracking the cyanoacrylate oligomer to yield the polymerizable acrylate monomer.
5. The method of claim 1 , further comprising distilling the polymerizable acrylate monomer to yield a biocompatible monomer.
6. The method of claim 1 , further comprising dissolving the polymerizable acrylate monomer in a zero VOC solvent.
7. The method of claim 6 , wherein dissolving the polymerizable acrylate monomer in the zero VOC solvent comprises dissolving in the zero VOC solvent selected from the group consisting of acetone, methyl acetate, t-butyl acetate, p-chlorobenzotrifluoride, and combinations thereof.
8. The method of claim 1 , further comprising dissolving the polymerizable acrylate monomer in a biocompatible solvent.
9. The method of claim 8 , wherein dissolving the polymerizable acrylate monomer in the biocompatible solvent comprises dissolving in the biocompatible solvent selected from the group consisting of ethanol, water, dimethyl sulfoxide, propylene glycol, and combinations thereof.
10. The method of claim 1 , wherein contacting the carbohydrate with a protecting group comprises contacting with a protecting group selected from the group consisting of amide, ester, ether, silane, carbamate, ketal, acetal, hemiacetal, hemiketal, carbonate, and combinations thereof.
11. The method of claim 1 , wherein contacting the carbohydrate with a protecting group comprises contacting the carbohydrate with acetic anhydride.
12. The method of claim 1 , wherein contacting the carbohydrate with a protecting group yields the protected carbohydrate, the protected carbohydrate including one or more protecting groups;
the method further comprising removing the one or more protecting groups from the protected carbohydrate after the protected carbohydrate has been linked to the polymerizable acrylate group.
13. The method of claim 12 , wherein removing the one or more protecting groups from the protected carbohydrate comprises contacting the protected carbohydrate with hydrochloric acid, lipase AS Amano (LAS), or an esterase.
14. The method of claim 1 , wherein providing the carbohydrate comprises providing a carbohydrate that is not mannose or galactose.
15. The method of claim 1 , the method further comprising providing a cross-linking moiety to the polymerizable acrylate monomer.
16. The method of claim 1 , wherein converting the cyanoacrylate intermediate group yields a polymerizable cyanoacrylate having a structure selected from the group consisting of:
wherein R 1 , R 2 , R 3 , and R 4 are independently an alkyl, heterocycle, cycle, carbocycle, or any atom other than hydrogen.
17. A method for making a biocompatible polymerizable acrylate product, the method comprising:
providing a carbohydrate having a plurality of hydroxyl groups;
contacting the carbohydrate with a protecting group agent to yield a protected carbohydrate; and
linking a polymerizable acrylate group to the protected carbohydrate to yield a polymerizable acrylate monomer having a pendant carbohydrate moiety, wherein the step of linking the polymerizable acrylate group to the protected carbohydrate includes bonding a cyanoacrylate intermediate group to the protected carbohydrate and then converting the cyanoacrylate intermediate group to a polymerizable cyanoacrylate;
wherein the bonding of the cyanoacrylate intermediate group to the protected carbohydrate comprises:
contacting the protected carbohydrate with an acid halide to yield a beta halide protected carbohydrate;
contacting the beta halide protected carbohydrate with a cyanoacetate to yield a cyanoacrylate intermediate; and
condensing the cyanoacrylate to yield a cyanoacrylate oligomer; and
cracking the cyanoacrylate oligomer to yield the polymerizable acrylate monomer.
18. A method for making a biocompatible material providing a porous structure within which living tissue may grow, the method comprising:
providing a carbohydrate having a plurality of hydroxyl groups;
contacting the carbohydrate with a protecting group agent to yield a protected carbohydrate;
linking a polymerizable acrylate group to the protected carbohydrate to yield a polymerizable acrylate monomer having a pendant carbohydrate moiety, wherein the step of linking the polymerizable acrylate group to the protected carbohydrate includes bonding a cyanoacrylate intermediate group to the protected carbohydrate and then converting the cyanoacrylate intermediate group to a polymerizable cyanoacrylate;
combining the polymerizable cyanoacrylate with nanoparticles and/or microparticles;
polymerizing the polymerizable cyanoacrylate in the presence of the nanoparticles and/or microparticles; and
removing the nanoparticles and/or microparticles to yield a porous scaffold of the polymerized cyanoacrylate.
19. The method of claim 18 , wherein the polymerized cyanoacrylate is a hydrogel.
20. The method of claim 18 , wherein the nanoparticles and/or microparticles are selected from the group consisting of (poly)methylmethacrylate (PMMA), a salt, and wax, wherein the nanoparticles and/or microparticles are removed using a solvent in which the nanoparticles and/or microparticles are soluble, to yield the porous scaffold of the polymerized cyanoacrylate.
21. The method of claim 18 , wherein the nanoparticles and/or microparticles comprise wax, wherein the nanoparticles and/or microparticles are removed by melting.