Chronotherapeutic Ocular Delivery System Comprising a Combination of Prostaglandin and a Beta-Blocker for Treating Primary Glaucoma

• US 20090155338A1
• Filed: 09/11/2006
• Published: 06/18/2009
• Est. Priority Date: 09/21/2005
• Status: Abandoned Application

• Current Assignee: Aston University
• Original Assignee: Aston University
• Inventors: Gherghel, Doina, Conway, Barbara R.
• Application Number:
  US11/992,272
• Publication Number:
  US 20090155338A1
• Time in Patent Office: Days
• US Class Current: 424/428
• CPC Class Codes: A61K 31/535 having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
• CPC Class Codes: A61K 31/5575 having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha
• CPC Class Codes: A61K 9/0051 Ocular inserts, ocular implants
• CPC Class Codes: A61P 27/02 Ophthalmic agents

Abstract

Chronotherapeutic delivery system for treating primary open-angle glaucoma, comprising a delivery system incorporating pharmaceutical products for delivery to an eye in the treatment of primary open-angle glaucoma (POAG), comprising: (a) a biocompatible erodible material incorporating a therapeutically-effective amount of a prostaglandin analogue, and (b) a reservoir containing a therapeutically-effective amount of a beta-blocker, whereby, when the delivery system is placed in the eye the prostaglandin analogue is delivered gradually as the erodible material is eroded, and the beta-blocker is delivered rapidly when at least a predetermined portion of the erodible material has been eroded.

Claims

1. A delivery system incorporating pharmaceutical products for delivery to an eye in the treatment of primary open-angle glaucoma (POAG), comprising:

(a) a biocompatible erodible material incorporating a therapeutically-effective amount of a prostaglandin analogue, and

(b) a reservoir containing a therapeutically-effective amount of a beta-blocker,

whereby, when the delivery system is placed in the eye the prostaglandin analogue is delivered gradually as the erodible material is eroded, and the beta-blocker is delivered rapidly when at least a predetermined portion of the erodible material has been eroded.

2. A delivery system according to claim 1, wherein the prostaglandin analogue and beta-blocker are located in separate layers.

3. A delivery system according to claim 1, wherein the rate of erosion of the erodible material is such that the erosion is completed during periods of high intraocular pressure and low ocular blood flow.

4. A delivery system according to claim 1, further comprising a layer of a biodegradable polymer separating the erodible material incorporating the prostaglandin analogue and the reservoir containing the beta-blocker, wherein at least a predetermined portion of the biodegradable polymer is biodegraded prior to the delivery of the beta-blocker.

5. A delivery system according to claim 1, wherein the reservoir containing the beta-blocker has upper, lower and side surfaces, and the or each side surface is sealed with an insulating support to inhibit premature leakage of the beta-blocker.

6. A delivery system according to claim 5, further comprising a barrier layer of a biodegradable polymer or a non-biodegradable polymer located on the lower surface of the reservoir containing the beta-blocker while the erodible material incorporating the prostaglandin analogue is located on the upper surface of the reservoir, or vice versa.

7. A delivery system according to claim 2, wherein the erodible material comprises a semi-permeable membrane to delay the delivery of the beta-blocker.

8. A delivery system according to claim 1, wherein the beta-blocker is delivered when substantially all of the erodible material has been eroded.

9. A delivery system according to claim 1, wherein the erodible material comprises a polymeric material.

10. A delivery system according to claim 9, wherein the polymeric material is selected from polyethylene oxide (PEO), poly(alkyl) cyanoacrylates, and co-polymers of methyl vinyl ether and maleic anhydride, poly(alkyl cyanoacrylates), copolymers of polylactic and glycolic acid, or copolymers of polyethylene oxide and a methacrylic acid polymer.

11. A delivery system according to claim 1, wherein the prostaglandin analogue is selected from latanoprost, bimatoprost, travoprost and unoprostone isopropyl.

12. A delivery system according to claim 1, wherein the reservoir comprises a material selected from glass, metal, ceramics, polyvinyl alcohol (PVA), cross-linked polyvinyl alcohol, polyvinyl acetate, polyvinylbutyrate, cross-linked polyvinyl butyrate, ethylene ethylacrylate copolymer, polyethyl hexylacrylate, polyvinyl chloride, polyvinyl acetals, plasticised ethylene vinylacetate copolymer, ethylene vinylchloride copolymer, polyvinyl esters, polyvinylformal, polyamides, polymethylmethacrylate, polybutylmethacrylate, plasticised polyvinyl chloride, plasticised nylon, plasticised soft nylon, plasticised polyethylene terephthalate, natural rubber, polyisoprene, polyisobutylene, polybutadiene, polyethylene, polytetrafluoroethylene, polyvinylidene chloride, polyacrylonitrile, cross-linked polyvinylpyrrolidone, polytrifluorochloroethylene, chlorinated polyethylene, poly(1,4′

-isopropylidene diphenylene carbonate), vinylidene chloride, acrylonitrile copolymer, vinyl chloride-diethyl fumerale copolymer, butadiene/styrene copolymers, silicone rubbers, medical grade polydimethylsiloxanes, ethylene-propylene rubber, silicone-carbonate copolymers, vinylidene chloride-vinyl chloride copolymer, vinyl chloride-acrylonitrile copolymer and vinylidene chloride-acrylonitride copolymer;

non-biodegradable polymers such as polymethylmethacrylate, a silicone elastomer, or silicone rubber, polyolefins, homopolymers, and copolymers of vinyl acetate, polyvinylchlorides, homopolymers and copolymers of acrylates, polyurethanes, polyvinylpyrrolidone, 2-pyrrolidone, polyacrylonitrile butadiene, polycarbonates, polyamides, fluoropolymers, polystyrenes, homopolymers and copolymers of styrene acrylonitrile, cellulose acetate, homopolymers and copolymers of acrylonitrile butadiene styrene, polymethylpentene, polysulfones, polyesters, polyimides, natural rubber, polyisobutylene and polymethylstyrene; and

synthetic biodegradable polymers such as polyesters of molecular weight from about 4,000 to about 100,000, homopolymers and copolymers of (poly)lactic acid and (poly)glycolic acid, such as polylactic glycolic acid copolymer (PLGA), polycaprolactone, homopolymers and copolymers of polyanhydrides, bis(p-anhydride) and poly(p-carboxyphenoxy) alkyl, homopolymers and copolymers of dicarboxylic acids, polymeric fatty acid dimer compounds, poly(alkyl-2-cyanoacrylate) such as poly(hexyl-2-cyanoacrylate), collagen (gelatin), polyacetals, divinyloxyalkylenes, polydihydropyrans, polyphosphazenes, homopolymers and copolymers of amino acids, polydioxinones, polyalkylcyano acetates, polysaccarides and their derivatives, cellulose and hydroxymethyl cellulose.

13. A delivery system according to claim 1, wherein the beta-blocker is betaxolol or a salt thereof, or carteolol hydrochloride, levobunolol hydrochloride, metipranolol, or timolol maleate.

14. A delivery system according to claim 4, wherein the biodegradable polymer is polylactic glycolic acid copolymer (PLGA).

15. A delivery system according to claim 6, wherein the barrier layer comprises either PLGA or polypropylene.

16. A delivery system according to claim 1, wherein the erodible material further comprises a mucoadhesive polymer.

18. A method of treating or preventing primary open-angle glaucoma in a mammal, comprising administering to the mammal a therapeutic amount of one or more prostaglandin analogues or beta-blockers via a delivery system according to claim 1.

20. A process for the preparation of a delivery system according to claim 1, comprising the steps of:

(a) dissolving a formulation containing the prostaglandin analogue in a solvent;

(b) adding this solution to the erodible material;

(c) removing the solvent;

(d) compressing the resultant powder into discs;

(e) dissolving a formulation containing the beta-blocker in a solvent;

(f) adding this solution to the reservoir;

(g) removing the solvent;

(h) compressing the resultant powder into discs;

(i) combining discs from steps (d) and (h).

21. A process according to claim 20, further comprising the step of incorporating a layer of biodegradable polymer separating the erodible material incorporating the prostaglandin analogue and the reservoir containing the beta-blocker.

17. A delivery system incorporating pharmaceutical products for delivery to an eye in the treatment of primary open-angle glaucoma (POAG), comprising:

(a) a layer of PEO incorporating a therapeutically-effective amount of latanoprost;

(b) a layer of PVA containing a therapeutically-effective amount of betaxolol;

(c) a layer of PLGA separating the PEO and PVA layers;

(d) a polypropylene insulating support located on the side surface(s) of the PVA layer;

(e) a barrier layer of PLGA or polypropylene located on the lower surface of the reservoir containing the betaxolol while the layer of PEO incorporating the latanoprost is located on the upper surface of the layer of PVA, or vice versa;

(f) a polyacrylic acid mucoadhesive polymer,

whereby, when the delivery system is placed in the eye the latanoprost is delivered gradually as the PEO is eroded, and the betaxolol is delivered rapidly when at least a predetermined portion of the PEO has been eroded.

19. (canceled)