Graft polymerization of substrate surfaces

• US 6,358,557 B1
• Filed: 09/10/1999
• Issued: 03/19/2002
• Est. Priority Date: 09/10/1999
• Status: Expired due to Term

• Current Assignee: Surgical Specialties Corporation Limited (Ssc Holdco Ltd)
• Original Assignee: STS Biopolymers Inc. (Angiotech Pharmaceuticals Incorporated)
• Inventors: Wang, Guo-Bin, Zhang, Xianping
• Primary Examiner(s): Beck, Shrive P.
• Assistant Examiner(s): Michener, Jennifer Kolb
• Application Number:
  US09/394,577
• Time in Patent Office: 921 Days
• Field of Search: 427/2.24, 427/2.25, 427/2.28, 427/2.3, 427/2.31, 427/487, 427/372.2, 427/301, 427/302, 427/303, 427/399, 427/406
• US Class Current: 427/2.24
• CPC Class Codes: A61L 29/085 Macromolecular materials
• CPC Class Codes: B05D 1/18 performed by dipping

Abstract

The invention includes a method of coating a substrate, comprising exposing a substrate to an initiator capable of initiating a graft polymerization reaction on the substrate, to generate reactive radical sites on the surface of the substrate; contacting the substrate with a composition comprising one or more monomers in a medium which has different hydrophilicity compared to the substrate, and grafting monomer molecules onto the substrate by forming covalent bonds between monomer molecules and the substrate at reactive radical sites on the substrate surface. With the invention, novel coated articles can be obtained which are particularly usefull as medical products such as catheters.

Claims

1. A method of coating a substrate, comprising:

exposing a substrate to an initiator in solution capable of initiating a graft polymerization reaction on the substrate, to generate reactive radical sites on the surface of the substrate;

contacting the exposed substrate having reactive radical sites with a composition comprising one or more monomers in a medium which has reversed phase properties compared to the substrate, in terms of hydrophilicity and further comprising a solute in an amount sufficient to induce a salting-out effect; and

graft polymerizing onto the substrate by forming covalent bonds between monomer molecules and the substrate at reactive radical sites on the substrate surface.

2. The method of claim 1, further comprising mixing the composition so that a plurality of said molecules remain in proximity to said reactive radical site.

3. The method of claim 1, wherein the monomers are grafted onto the substrate at a pressure less than about 50 atmospheres.

4. The method of claim 1, wherein the monomers are grafted onto the substrate at a temperature from about 10°

C. to about 100°

C.

5. The method of claim 1, wherein the substrate is selected from the group consisting of solid synthetic polymers and solid natural polymers.

6. The method of claim 5, wherein the substrate is selected from the group consisting of polyolefin, silicone polymer, acrylic polymer, acrylic copolymer, polyesteracrylate, polyestermethacrylate, fluoropolymer, vinyl polymer, vinyl monomer-containing copolymer, natural rubber, synthetic rubber, polyurethane, polyamide, polyester, epoxy polymer, wool, cotton, silk, rayon, and cellulose.

7. The method of claim 6, wherein the substrate is selected from the group consisting of polyethylene, polypropylene, polyisobutylene, ethylene-alphaolefin copolymer, polyacrylonitrile, poly(methyl methacrylate), poly(ethyl methacrylate), poly(ethyl acrylate), poly(tetrafluoroethylene), poly(chlorotrifluoroethylene), fluorinated ethylene-propylene, poly(vinyl fluoride), poly(vinyl chloride), poly(vinyl methyl ether), polystyrene, poly(vinyl acetate), poly(vinyl ketone), ABS rubber, latex rubber, butadiene-styrene copolymer, polyisoprene, polybutadiene, butadiene-acrylonitrile copolymer, polychloroprene polymer, polyisobutylene rubber, ethylene-propylenediene copolymer, poly(isobutylene/isoprene), polyetherurethane, polyesterurethane, polycarbonateurethane and polysiloxaneurethane, Nylon 6, Nylon 66, Nylon 10, Nylon 11, modified cellulose, polyacrylamide, poly(2-hydroxyethylacrylate), poly(N,N′

-dimethylacrylamide), poly(acrylic acid), polymethacrylic acid, poly(N-vinylpyrrolidone), polyvinylpyridine, polymaleic acid, poly(2-hydroxyethyl fumarate), maleic anhydride, starch, and poly(vinyl alcohol).

8. The method of claim 1, wherein the medium is a hydrophilic aqueous solution.

9. The method of claim 8, wherein the solute is selected from the group consisting of water soluble chloride salt, water soluble phosphate salt, or water soluble acetate salt.

10. The method of claim 8, wherein the solute is selected from the group consisting of water soluble sodium salt, water soluble potassium salt, and water soluble ammonium salt.

11. The method of claim 8, wherein the solute is selected from the group consisting of sodium chloride, potassium chloride, ammonium chloride.

12. The method of claim 8, wherein the solute is present in a concentration greater than about 0.5 moles per liter.

13. The method of claim 12, wherein the solute is present in a concentration greater than about 2 moles per liter.

14. The method of claim 1, wherein the medium is hydrophobic, and comprises an organic solvent.

15. The method of claim 1, wherein the solution comprises a water soluble polymer.

16. The method of claim 15, wherein the solute is a non-ionic species with high solubility in the medium.

17. The method of claim 16, wherein the non-ionic species is and poly(vinylpyrrolidone).

18. The method of claim 14, wherein the medium comprises a solvent selected from the group consisting of toluene, hexane, cyclohexane, and mixtures thereof.

19. The method of claim 1, wherein the initiator is selected from the group consisting of peroxide initiators, azo initiators, redox initiators, and photoinitiators/photosensitizers which can be thermally initiated.

20. The method of claim 19, wherein the initiator is a peroxide initiator selected from the group consisting of peroxyester, peroxyketal, peroxydicarbonate, ketone peroxide, dialkyl peroxide, diacyl peroxide, an inorganic peroxide, and mixtures thereof.

21. The method of claim 19, wherein the initiator is selected from the group consisting of 1,1-dimethyl-3-hydroxybutyl peroxyneodecanoate, α

-cumyl peroxyneodecanoate, α

-cumyl peroxyneoheptanoate, t-amyl peroxyneodecanoate, t-butyl peroxyneodecanoate, t-amyl peroxypivalate, t-butyl peroxypivalate, 2,5-dimethyl 2,5-di(2-ethylhexanoylperoxy)hexane, t-butylperoxy-2-ethylhexanoate, t-butylperoxyacetate, t-amylperoxyacetate, t-butylperbenzoate, t-amylperbenzoate, t-butyl-1-(2-ethylhexyl)monoperoxycarbonate, 1,1-di(t-butylperoxy)-3,3,5-trimethyl-cyclohexane, 1,1-di(t-butylperoxy)-cyclohexane, 1,1-di(t-amylperoxy)-cyclohexane, ethyl-3,3-di(t-butylperoxy)-butyrate, ethyl-3,3-di(t-amylperoxy)-butylperoxy)-butylrate, di(n-propyl)peroxydicarbonate, di(sec-butyl)perosydicarbonate, di(2-ethylhexyl)peroxydicarbonate, 2,4-pentanedione peroxide, cumene hydroperoxide, butyl hydroperoxide, amyl hydroperoxide, dicumyl peroxide, dibutylperoxide, diamylperoxide, decanoyl peroxide, lauroyl peroxide, benzoyl peroxide, hydrogen peroxide, potassium persulfate, and mixtures thereof.

22. The method of claim 19, wherein the initiator is an azo initiator selected from the group consisting of azobisisobutyronitrile, azobiscumene, azo-bisiso-1,1,1-tricyclopropylmethane, 4-nitrophenyl-azo-triphenylmethane phenyl-azo-triphenylmethane, and mixtures thereof.

23. The method of claim 19, wherein the initiator is a redox initiator selected from the group consisting of peroxide-amine systems, peroxide-metal ion systems, and boronalkyl-oxygen systems.

24. The method of claim 1, wherein the monomer is selected from the group consisting of hydrophilic monomers and hydrophobic monomers.

25. The method of claim 24, wherein the monomer comprises a hydrophilic monomer selected from the group consisting of hydroxyl substituted ester acrylate, ester methacrylate, 2-hydroxyethylacrylate, 2-hydroxypropylacrylate, 3-hydroxypropylacrylate, 2,3-dihydroxypropylacrylate, polyethoxyethylacrylate, polyethoxypropylacrylate, acrylamide, methacrylamide, N-methylacrylamide, N,N-dimethylacrylamide, N,N-dimethylmethacrylamide, N,N-dimethyl-aminoethyl, 2-acrylamido-2-methyl-1-propanesulfonic acid, N,N-diethyl-aminoethyl, 2-acrylamido-2-methyl-1-propanesulfonic acid, N-[3-dimethylamino)propyl]acrylamide, 2-(N,N-diethylamino)ethyl methacrylamide, polyethylene glycol acrylate, polyethylene glycol methacrylate, polyethylene glycol diacrylate, polyethylene glycol dimethacrylate;

polypropylene glycol acrylate, polypropylene glycol methacrylate, polypropylene glycol diacrylate, polypropylene glycol dimethacrylate;

acrylic acid, methacrylic acid, 2- and 4-vinylpyridine;

4- and 2-methyl-5-vinylpyridine, N-methyl-4-vinylpiperidine, 2-methyl-1-vinylimidazole, dimethylaminoethyl vinyl ether, N-vinylpyrrolidone, itaconic acid, crotonic acid, flumaric acid, maleic acid, and mixtures thereof.

26. The method of claim 24, wherein the monomer comprises a hydrophobic monomer selected from the group consisting of ester acrylates selected from the group consisting of methyl, ethyl, propyl, butyl, phenyl, benzyl, cyclohexyl, ethoxyethyl, methoxyethyl, ethoxypropyl, hexafluoroisopropyl and n-octyl-acrylates;

ester methacrylates selected from the group consisting of methyl, ethyl, propyl, butyl, phenyl, benzyl, cyclohexyl, ethoxyethyl, methoxyethyl, ethoxypropyl, hexafluoroisopropyl and n-octyl-methacrylates;

acrylamides;

methacrylamides;

dimethyl fumarate;

dimethyl maleate;

diethyl fumarate;

methyl vinyl ether;

ethoxyethyl vinyl ether;

vinyl acetate;

vinyl propionate;

vinyl benzoate;

acrylonitrile;

styrene;

alpha-methylstyrene;

1-hexene;

vinyl chloride;

vinyl methyl ketone;

vinyl stearate;

2-hexene;

2-ethylhexyl methacrylate, and mixtures thereof.

30. The method of claim 1, wherein the composition further comprises a water soluble polymer.

31. The method of claim 30, wherein the water soluble polymer is poly(vinylpyrollidone).

32. The method of claim 31, wherein the poly(vinylpyrollidone) is present in a concentration from about 0.01 weight percent to about 3.0 weight percent.

33. The method of claim 30, wherein the substrate is silicone;

the initiator is an organic peroxide solution in tetrahydrofuran (THF);

the medium comprises from about 3% w/w to about 6% w/w acrylamide derivatives, from about 0.1% w/w to about 0.4% w/w diacrylate crosslinker, from about 10% w/w to about 20% w/w sodium chloride and from about 0.01% w/w to about 0.03% w/w poly(vinylpyrrolidone); and

,

the reaction is allowed to proceed at a temperature from about 80°

C. to about 95°

C. at atmospheric pressure.

34. The method of claim 30, wherein the substrate is silicone;

the initiator is an organic peroxide solution in tetrahydrofuran (THF);

the medium comprises from about 1.0% w/w to about 3.0% w/w acrylamide derivatives, from about 3.0% w/w to about 5% w/w polyethylene glycol acrylate, from about 10% w/w to about 20% w/w sodium chloride and from about 1.0% w/w to about 3.0% w/w poly(vinylpyrrolidone); and

the reaction is allowed to proceed at a temperature from about 80°

C. to about 95°

C. at atmospheric pressure.

35. The method of claim 30, wherein the substrate is polyethylene;

the medium comprises from about 20% w/w to about 40% w/w acrylamide, from about 1% w/w to about 3% w/w polyvinylpyrrolidone, and from about 10% w/w to about 20% w/w sodium chloride; and

the reaction is allowed to proceed at a temperature from about 80°

C. to about 95°

C. at atmospheric pressure.

36. The method of claim 1, wherein the substrate is selected from the group consisting of silicone, polyethylene, polyamide and latex, and wherein the grafting coats the substrate surface with a coating having characteristics selected from the group consisting of lubricious, hydrophilic and elastic properties.

37. The method of claim 1, further comprising attaching to the coated substrate a biological agent selected from the group consisting of penicillins, cephalosporins, fluoroquinolones, aminoglycosides, silver compounds, phenols, and biguanides.

27. A method of coating a substrate, comprising:

exposing a substrate to an initiator in solution capable of initiating a graft polymerization reaction on the substrate, to generate reactive radical sites on the surface of the substrate;

contacting the substrate with a composition comprising one or more monomers in a medium which has reversed phase properties compared to the substrate, in terms of hydrophilicity and a concentration of a solute sufficient to induce a salting-out effect, while mixing the composition;

graft polymerizing onto the substrate by forming covalent bonds between monomer molecules and the substrate at reactive radical sites on the substrate surface; and

contacting the substrate with a cross-linking agent.

28. The method of claim 27, wherein the cross-linking agent is selected from the group consisting monomers having di- or multi-unsaturated functional groups.

29. The method of claim 28, wherein the cross-linking agent is selected from the group consisting of diacrylates of poly(ethylene glycol), diacrylates of poly(propylene glycol), dimethylacrylates of poly(ethylene glycol), dimethylacrylates of poly(propylene glycol), trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, di-trimethylolpropane, tetraacrylate, pentaerythritol tetraacrylate, tetramethacrylate, divinylbenzene, divinyl sulfone, silicone-containing diacrylates and dimethacrylates, and mixtures thereof.

38. A method of coating a substrate, comprising:

exposing a substrate to an initiator in solution capable of initiating a graft polymerization reaction on the substrate, to generate reactive radical sites on the surface of the substrate;

contacting the substrate with a composition comprising one or more monomers in a medium and a concentration of a solute sufficient to induce a salting-out effect; and

graft polymerizing onto the substrate at a pressure less than about 50 atmospheres by forming covalent bonds between monomer molecules and the substrate at reactive radical sites on the substrate surface.

39. The method of claim 38, wherein said graft polymerization is accomplished at a pressure less than about 10 atmospheres.