PROCESS FOR FORMING CLEAR, WETTABLE SILICONE HYDROGEL ARTICLES

• US 20070138692A1
• Filed: 10/31/2006
• Published: 06/21/2007
• Est. Priority Date: 09/06/2002
• Status: Abandoned Application

• Current Assignee: Johnson & Johnson Vision Care Incorporated (Johnson & Johnson)
• Original Assignee: Johnson & Johnson Vision Care Incorporated (Johnson & Johnson)
• Inventors: Zanini, Diana, Ford, James, Altheim, Karen
• Application Number:
  US11/555,133
• Publication Number:
  US 20070138692A1
• Time in Patent Office: Days
• US Class Current: 264/236
• CPC Class Codes: A61L 27/18 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• CPC Class Codes: B29D 11/00134 Curing of the contact lens material
• CPC Class Codes: C08L 51/085 on to polysiloxanes
• CPC Class Codes: C08L 83/04 Polysiloxanes
• CPC Class Codes: G02B 1/043 Contact lenses

Abstract

The present invention is a process for forming ophthalmic devices such as contact lenses, comprising at least one silicone containing component, at least one hydrophilic component, at least one hydrophilic polymer and at least one diluent with a Hansen solubility parameter of about 2 to about 7. The processing of the ophthalmic device may be done using only aqueous solutions.

Claims

1. A process comprising the steps of curing a reactive mixture comprising at least one silicone containing component, at least one hydrophilic component and at least one diluent having a Hansen solubility parameter, δ

p between about 2 and about 7 to form an ophthalmic device having an advancing contact angle of less than about 80°

; and

removing said diluent with an aqueous solution.

2. The process of claim 1 wherein said diluent is selected from the group consisting of diisopropylaminoethanol, dipropylene glycol methyl ether, 1-octanol, 1-pentanol, 2-pentanol, 1-hexanol, 2-hexanol, 2-octanol, 3-methyl-3-pentanol, tert-amyl alcohol, tert-butanol, 2-butanol, 1-butanol, 2-methyl-2-pentanol, 2-propanol, 1-propanol, ethanol, 2-ethyl-1-butanol, 1-tert-butoxy-2-propanol, 3,3-dimethyl-2-butanol, tert-butoxyethanol, tripropylene glycol methyl ether, decanoic acid, octanoic acid, hexanoic acid, dodecanoic acid, 2-(diisopropylamino)ethanol and mixtures thereof.

3. The process of claim 1 wherein said diluent is selected from the group consisting of alcohols having 2 to 20 carbons and a carbon:

oxygen from hydroxyl ratio of up to about 8;

about 1, amides having 10 to 20 carbon atoms derived from primary amines and carboxylic acids having 6 to 20 carbon atoms and mixtures thereof.

4. The process of claim 1 wherein said diluent is selected from the group consisting of alcohols having 5 to 20 carbons having a carbon:

oxygen from hydroxyl ratio of about 3;

abut 1 to about 6;

about 1, carboxylic acids having 6 to 18 carbon atoms and amines having 6-14 carbon atoms and mixtures thereof.

5. The process of claim 1 wherein said removing step is conducted at a temperature of about to about 20°

C. to about 95°

C.

6. The process of claim 1 wherein said removing step is conducted at a temperature of about 70°

C. to about 95°

C.

7. The process of claim 1 wherein said reactive mixture comprises from about 30 to about 85 weight percent silicone containing component(s) based upon all reactive components in the reaction mixture.

8. The process of claim 1 wherein said reactive mixture comprises from about 45 to about 75 weight percent weight percent silicone containing component(s) based upon all reactive components in the reaction mixture.

9. The process of claim 1 wherein said reactive mixture comprises from about 10 to about 60 weight percent hydrophilic component(s), based upon all reactive components in the reaction mixture.

10. The process of claim 1 wherein said reactive mixture comprises from about 20 to about 50 weight percent hydrophilic component(s), based upon all reactive components in the reaction mixture.

11. The process of claim 1 wherein said silicone containing component comprises at least one mono-functional silicone monomer.

12. The process of claim 11 wherein said at least one mono-functional silicone is selected from the group consisting of mono-(2-hydroxy-3-methacryloxypropyl)-propyl ether terminated polydimethylsiloxane, monomethacryloxypropyl terminated mono-n-butyl terminated polydimethylsiloxanes, 2-methyl-,2-hydroxy-3-[3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propoxy]propyl ester and mixtures thereof.

13. The process of claim 1 wherein said hydrophilic component comprises at least one hydrophilic monomer selected from the group consisting of N,N-dimethyl acrylamide, 2-hydroxyethyl acrylate, glycerol methacrylate, 2-hydroxyethyl methacrylamide, N-vinylpyrrolidone, N-vinyl methacrylamide, 2-hydroxyethyl methacrylate, polyethyleneglycol monomethacrylate, polyvinylpyrrolidone and mixtures thereof.

14. The process of claim 1 wherein said hydrophilic component comprises at least one hydrophilic monomer selected from the group consisting of N,N-dimethyl acrylamide, N-vinylpyrrolidone, 2-hydroxyethyl methacrylate and mixtures thereof.

15. The process of claim 1 wherein the reactive mixture further comprises at least one hydrophilic polymer.

16. The process of claim 15 wherein the at least one hydrophilic polymer is present in the reactive mixture in an amount between about 1 to about 15 weight % of all reactive components in the reactive mixture.

17. The process of claim 15 composition of claim 15 wherein the at least one hydrophilic polymer is present in the reactive mixture in an amount between about 5 to about 17 weight % of all reactive components in the reactive mixture.

18. The process of claim 15 wherein the hydrophilic polymer comprises poly-N-vinylpyrrolidone.

19. The process of claim 1 wherein said diluent is selected from the group consisting of tripropylene glycol methyl ether, 1-pentanol, 3-methyl-3-pentanol, 1-pentanol, 2-pentanol, t-amyl alcohol, tert-butanol, 2-butanol, 1-butanol, 2-methyl-2-pentanol, 2-ethyl-1-butanol, 3,3-dimethyl-2-butanol, 2-octyl-1-dodecanol, decanoic acid, hexanoic acid, octanoic acid, dodecanic acid, and mixtures thereof.

20. The process of claim 19 wherein said diluent is a mixture comprising a co-diluent selected from the group consisting of decanoic acid, hexanoic acid, octanoic acid, dodecanoic acid, and mixtures thereof.

21. The process of claim 1 wherein said at least one diluent comprises tripropylene glycol methyl ether.

22. The process of claim 21 wherein said diluent further comprises at least one co-diluent selected from the group consisting of decanoic acid, hexanoic acid, octanoic acid, dodecanoic acid, mixtures thereof.

23. A method comprising the steps of (a) forming a reactive mixture by mixing reactive components comprising at least one high molecular weight hydrophilic polymer and an effective amount of at least one hydroxyl-functionalized silicone-containing monomer in the presence of at least one diluent that is inert and easily displaceable with water and (b) curing the product of step (a) to form a biomedical device.

24. A method comprising the steps of (a) forming a reactive mixture by mixing reactive components comprising at least one high molecular weight hydrophilic polymer, at least one siloxane containing macromer and an effective amount of at least one compatibilizing component in the presence of at least one diluent that is inert and easily displaceable with water and (b) curing the product of step (a) to form a biomedical device.