Multiple phase cross-linked compositions and uses thereof

• US 20060204582A1
• Filed: 05/15/2006
• Published: 09/14/2006
• Est. Priority Date: 06/19/2000
• Status: Abandoned Application

• Current Assignee: Rutgers University
• Original Assignee: Rutgers University
• Inventors: Stein, Stanley, Qiu, Bo
• Application Number:
  US11/434,023
• Publication Number:
  US 20060204582A1
• Time in Patent Office: Days
• US Class Current: 424/486
• CPC Class Codes: A61K 47/34 Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers A61K47/10 takes precedence
• CPC Class Codes: A61K 9/0024 Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue compositions for intravenous administration, normal injectable solutions or dispersions for, e.g. subcutaneous administration A61K9/0019; brain implants A61K9/0085; (coated) prostheses, catheters or stents A61L
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: A61P 3/02 Nutrients, e.g. vitamins, minerals
• CPC Class Codes: A61P 31/10 Antimycotics
• CPC Class Codes: A61P 31/18 for HIV
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: A61P 5/00 Drugs for disorders of the endocrine system
• CPC Class Codes: A61P 7/00 Drugs for disorders of the blood or the extracellular fluid

Abstract

The present invention is directed to pharmaceutical compositions, and method for preparing pharmaceutical compositions, comprising a cross-linked matrix physically entrapping at least one therapeutic agent. The matrix may comprise one or more phases in addition to an aqueous phase, such as a solid and/or oil phase. The matrix of the invention has at least one controlled release in-vivo kinetic profile, and may have additional profiles for the same agent. The matrix may also comprise more than one therapeutic agent, and each additional therapeutic agent may have one or more controlled release in-vivo kinetic profile.

Claims

1. A pharmaceutical composition comprising a matrix capable of delivering at least one therapeutic agent to a bodily compartment under controlled release conditions, said matrix comprising a homogenous mixture of an aqueous phase and at least one other phase, at least one therapeutic agent present in at least one of said phases, and at least one cross-linked polymer physically entrapping said at least one therapeutic agent.

2. The pharmaceutical composition of claim 1 wherein said at least one other phase is a solid phase, an oil phase, or a combination thereof.

3. The pharmaceutical composition of claim 2 wherein said oil phase and said aqueous phase are in the form of an emulsion.

4. The pharmaceutical composition of claim 1 wherein said polymer comprises a backbone selected from the group consisting of poly(alkylene oxide), carboxymethylcellulose, dextran, modified dextran, polyvinyl alcohol, N-(2-hydroxypropyl)methacrylamide, polyvinyl pyrrolidone, poly-1,3-dioxolane, poly-1,3,6-trioxane, polypropylene oxide, a copolymer of ethylene and maleic acid anhydride, a polyactide/polyglycolide copolymer, a polyaminoacid, a copolymer of poly(ethylene glycol) and an amino acid, and a polypropylene oxide/ethylene oxide copolymer.

5. The pharmaceutical composition of claim 1 wherein said polymer comprises at least two functional or reactive groups.

6. The pharmaceutical composition of claim 5 wherein said functional groups are amino, carboxyl, thiol, hydroxyl, or any combination thereof.

7. The pharmaceutical composition of claim 6 wherein said polymer is an poly(alkylene oxide) derivative.

8. The pharmaceutical composition of claim 7 wherein said poly(alkylene oxide) derivative is selected from the group consisting of α

,ω

dihydroxy-poly(ethylene glycol) and α

,ω

-diamino-poly(ethylene glycol).

9. The pharmaceutical composition of claim 6 wherein said functional groups are thiol groups.

10. The pharmaceutical composition of claim 9 wherein said polymer is prepared from α

,ω

-diamino-poly(ethylene glycol) and thiomalic acid;

α

,ω

dihydroxy-poly(ethylene glycol) and thiomalic acid;

or α

,ω

dicarboxy-PEG-subunits and lysine, wherein free carboxy groups on said lysine are derivatized to provide thiol groups.

11. The pharmaceutical composition of claim 9 wherein said thiol groups on said polymer are cross-linked by thioether or disulfide bonds.

12. The pharmaceutical composition of claim 9 wherein said thiol groups on said polymer are sterically hindered.

13. The pharmaceutical composition of claim 1 wherein said at least one therapeutic agent is selected from the group consisting of a small-molecule drug, a protein, a nucleic acid and a polysaccharide.

14. The pharmaceutical composition of claim 13 wherein said small molecule drug is selected from the group consisting of an anticancer drug, a cardiovascular drug, an antibiotic, an antifungal, an antiviral drug, an AIDS drug, an HIV-1 protease inhibitor, a reverse transcriptase inhibitor, an anti-nociceptive drug, a hormone, a vitamin, an anti-inflammatory drug, an angiogenesis drug, and an anti-angiogenesis drug.

15. The pharmaceutical composition of claim 1 wherein said matrix has at least one controlled release in-vivo kinetic profile selected from the group consisting of zero order, pseudo zero order, and first order.

16. The pharmaceutical composition of claim 1 wherein said controlled release conditions is a constant rate of release.

17. The pharmaceutical composition of claim 1 wherein said matrix further comprises an excipient.

18. The pharmaceutical composition of claim 17 wherein said excipient is selected from the group consisting of a monovalent metal ion, a polyvalent metal ion, an anionic polymer, a cationic polymer, a nonionic polymer, surfactant, and a protein.

19. A method for preparing the pharmaceutical composition of claim 1 comprising the steps of

i) preparing a mixture comprising at least one therapeutic agent and at least two phases one of which is an aqueous phase, said aqueous phase comprising a polymer having at least two functional groups thereon;

ii) cross-linking said polymer under conditions to form a cross-linked matrix having said therapeutic agent trapped therein.

20. The method of claim 19 wherein said functional groups are thiol groups.

21-37. -37. (canceled)