DRUG DELIVERY DEVICES

• US 20080145405A1
• Filed: 12/15/2006
• Published: 06/19/2008
• Est. Priority Date: 12/15/2006
• Status: Abandoned Application

• Current Assignee: Bausch & Lomb Incorporated (Bausch Health Cos., Inc.)
• Original Assignee: Bausch & Lomb Incorporated (Bausch Health Cos., Inc.)
• Inventors: Kunzler, Jay F., Jani, Dharmendra M.
• Application Number:
  US11/611,674
• Publication Number:
  US 20080145405A1
• Time in Patent Office: Days
• US Class Current: 424/427
• CPC Class Codes: A61F 9/0017 implantable in, or in contact with, the eye, e.g. ocular inserts
• CPC Class Codes: A61K 47/32 Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers , poly(meth)acrylates, or polyvinyl pyrrolidone
• CPC Class Codes: A61K 9/0051 Ocular inserts, ocular implants

Abstract

A method for making an ocular drug delivery device, the method comprising providing a drug delivery device comprising a core comprising a therapeutically effective amount of one or more pharmaceutically active agents and a first polymeric material, and a shell covering the core, the shell comprising a second polymeric material which is permeable to passage of the active agent, wherein the first and/or second polymeric material include one or more contaminants and wherein the drug delivery device is sized and configured for implantation or injection in eye tissue; and subjecting the drug delivery device to a supercritical fluid to remove the contaminants.

Claims

1. A method for making an ocular drug delivery device, the method comprising providing a drug delivery device comprising (a) a core comprising a therapeutically effective amount of one or more pharmaceutically active agents and a first polymeric material, and a shell covering the core, the shell comprising a second polymeric material which is permeable to passage of the one or more pharmaceutically active agents, wherein the first and/or second polymeric material include one or more contaminants and wherein the drug delivery device is sized and configured for implantation or injection in eye tissue;

and (b) subjecting the drug delivery device to a supercritical fluid to remove the contaminants.

2. The method of claim 1, wherein the first polymeric material and the second polymeric material are the same material.

3. The method of claim 1, wherein the first polymeric material and the second polymeric material are different material.

4. The method of claim 1, wherein the first polymeric material comprises a reaction product of a monomeric mixture comprising one or more acrylate ester and/or methacrylate ester-containing monomers and one or more acrylamido-containing monomers.

5. The method of claim 4, wherein the one or more acrylate ester and/or methacrylate ester-containing monomers is represented by general formula I:

6. The method of claim 4, wherein the one or more acrylate ester and/or methacrylate ester-containing monomers is selected from the group consisting of a methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, iso-butyl acrylate, t-butyl acrylate, n-hexyl acrylate, 2-ethylbutyl acrylate, 2-ethylhexyl acrylate, cyclopropyl acrylate, cyclobutyl acrylate, cyclohexyl acrylate, benzyl acrylate, 2-phenoxyethyl acrylate, phenyl acrylate, 2-phenylethyl acrylate, 3-phenylpropyl acrylate, 3-phenoxypropyl acrylate, 4-phenylbutyl acrylate, 4-phenoxybutyl acrylate, 4-methylphenyl acrylate, 4-methylbenzyl acrylate, 2-2-methylphenylethyl acrylate, 2-3-methylphenylethyl acrylate, 2-methylphenylethyl acrylate and mixtures thereof.

7. The method of claim 4, wherein the one or more acrylamido-containing monomers is represented by the general formulae II and III:

8. The method of claim 4, wherein the one or more acrylamido-containing monomer is selected from the group consisting of acrylamide, N-methylacrylamide, N-ethylacrylamide, N-propylacrylamide, N-isopropylacrylamide, N-butylacrylamide, N,N-dimethylacrylamide, N,N-diethylacrylamide, N,N-dipropylacrylamide, N,N-dibutylacrylamide, N,N-methylethylacrylamide, N,N-methylpropylacrylamide, N,N-ethylpropylacrylamide, N,N-ethylbutylacrylamide, N,N-propylbutylacrylamide, N-cyclopropylacrylamide, N-cyclobutylacrylamide and mixtures thereof.

9. The method of claim 4, wherein the monomeric mixture further comprises one or more crosslinking agents.

10. The method of claim 9, wherein the crosslinking agent is selected from the group consisting of tripropylene glycerol diacrylate, ethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, poly(ethylene glycol diacrylate), methylene bis acrylamide and mixtures thereof.

11. The method of claim 1, wherein the second polymeric material comprises a reaction product of a monomeric mixture comprising one or more acrylate ester and/or methacrylate ester-containing monomers and one or more acrylamido-containing monomers.

12. The method of claim 11, wherein the one or more acrylate ester and/or methacrylate ester-containing monomers is represented by general formula I:

13. The method of claim 11, wherein the one or more acrylate ester and/or methacrylate ester-containing monomers is selected from the group consisting of a methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, n-butyl acrylate, iso-butyl acrylate, t-butyl acrylate, n-hexyl acrylate, 2-ethylbutyl acrylate, 2-ethylhexyl acrylate, cyclopropyl acrylate, cyclobutyl acrylate, cyclohexyl acrylate, benzyl acrylate, 2-phenoxyethyl acrylate, phenyl acrylate, 2-phenylethyl acrylate, 3-phenylpropyl acrylate, 3-phenoxypropyl acrylate, 4-phenylbutyl acrylate, 4-phenoxybutyl acrylate, 4-methylphenyl acrylate, 4-methylbenzyl acrylate, 2-2-methylphenylethyl acrylate, 2-3-methylphenylethyl acrylate, 2-methylphenylethyl acrylate and mixtures thereof.

14. The method of claim 11, wherein the one or more acrylamido-containing monomers is represented by the general formulae II and III:

15. The method of claim 11, wherein the one or more acrylamido-containing monomer is selected from the group consisting of acrylamide, N-methylacrylamide, N-ethylacrylamide, N-propylacrylamide, N-isopropylacrylamide, N-butylacrylamide, N,N-dimethylacrylamide, N,N-diethylacrylamide, N,N-dipropylacrylamide, N,N-dibutylacrylamide, N,N-methylethylacrylamide, N,N-methylpropylacrylamide, N,N-ethylpropylacrylamide, N,N-ethylbutylacrylamide, N,N-propylbutylacrylamide, N-cyclopropylacrylamide, N-cyclobutylacrylamide and mixtures thereof.

16. The method of claim 1, wherein the one or more pharmaceutically active agents is selected from the group consisting of an anti-glaucoma agent, anti-cataract agent, anti-diabetic retinopathy agent, thiol cross-linking agent, anti-cancer agent, immune modulator agent, anti-clotting agent, anti-tissue damage agent, anti-inflammatory agent, anti-fibrous agent, non-steroidal anti-inflammatory agent, antibiotic, anti-pathogen agent, piperazine derivative, cycloplegic agent, miotic agent, mydriatic agent and mixtures thereof.

17. The method of claim 1, wherein the one or more pharmaceutically active agents is selected from the group consisting of an anticholinergic, anticoagulant, antifibrinolytic, antihistamine, antimalarial, antitoxin, chelating agent, hormone, immunosuppressive, thrombolytic, vitamin, protein, salt, desensitizer, prostaglandin, amino acid, metabolite, antiallergenic and mixtures thereof.

18. The method of claim 1, wherein the drug delivery device comprises a pharmaceutically active salt, and the contaminants are hydrophobic.

19. The method of claim 1, wherein the supercritical fluid is selected from the group consisting of supercritical carbon dioxide, supercritical nitrous oxide, supercritical ethane and supercritical propane.

20. The method of claim 1, wherein the supercritical fluid comprises supercritical carbon dioxide.

21. A method for making an ocular drug delivery device, the method comprising providing a drug delivery device comprising (a) a core comprising a therapeutically effective amount of one or more pharmaceutically active agents and a first polymeric material, and (b) a shell covering the core, the shell comprising a second polymeric material which is permeable to passage of the one or more pharmaceutically active agents;

and removing contaminants from the device by subjecting the device to a supercritical fluid.