Prostaglandin conjugates and derivatives for treating glaucoma and ocular hypertension
View Patent ↗Prostaglandin conjugates and derivatives and methods for their use to treat glaucoma and/or lower intraocular pressure are disclosed. Additionally, ophthalmic pharmaceutical compositions useful in the treatment of eye diseases such as glaucoma and elevated intraocular pressure are disclosed. Such compositions comprise an effective amount of prostaglandin conjugates or derivatives of the present invention.
1. An ophthalmic pharmaceutical composition useful in the treatment of glaucoma and control of intraocular pressure, comprising an effective amount of a compound (I) of the following formula:
in which A is selected from the group consisting of:
where:
n is 1-6;
R 1 , R 2 , R 3 independently=OH or O—NO 2 ;
R 4 , R 5 independently=H, alkyl, or heteroalkyl; or R 4 and R 5 can combine to form cyclic alkyl or cyclic heteroalkyl; and
R 6 independently=H, NO 2 , organic nitrate, organic nitrite, metal —NO complex, sodium nitroprusside (SNP), dinitrosyl iron thiol complex (DNICs), N-nitrosamine, N-hydroxy-N-nitrosamine, N-nitrosimine, nitrosimine, C-nitroso, diazetine dioxide, furoxan, benzofuroxan, oxatriazole-5-imine, sydnonimine, oxime, hydroxylamine, N-hydroxyguanidine, or hydroxyurea; and
a pharmaceutically acceptable vehicle therefor.
2. The composition of claim 1 comprising a pharmaceutically acceptable salt of compound (I).
3. The composition of claim 1 further comprising a compound selected from the group consisting of:
ophthalmologically acceptable preservatives, surfactants, viscosity enhancers, penetration enhancers, gelling agents, hydrophobic bases, vehicles, buffers, sodium chloride, and water.
4. The composition of claim 1 wherein said composition comprises a plurality of glaucoma treatment agents.
5. The composition of claim 4 wherein at least one glaucoma treatment agent is selected from the group consisting of:
β-blockers, prostaglandin analogs, carbonic anhydrase inhibitors, α2 agonists, miotics, rho kinase inhibitors, serotonergic agonists, and neuroprotectants.
6. The composition of claim 1 wherein said composition comprises from about 0.01 percent weight/volume to about 5 percent weight/volume of said compound.
7. The composition of claim 1 wherein said composition comprises from about 0.05 percent weight/volume to about 2 percent weight/volume of said compound.
8. The composition of claim 1 wherein said compound is selected from the group consisting of: Isopropyl (Z)-7-((1R,2R,3R,5S)-3,5-bis(nitrooxy)-2-((R,E)-3-(nitrooxy)-4-(3-(trifluoromethyl)phenoxy)but-1-en-1-yl)cyclopentyl)hept-5-enoate and (Z)-2-((((Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((R,E)-3-hydroxy-4-(3-(trifluoromethyl)phenoxy)but-1-en-1-yl)cyclopentyl)hept-5-enoyl)oxy)methoxy)-1-(pyrrolidin-1-yl)diazene 1-oxide.
9. A method for lowering intraocular pressure comprising: applying a therapeutically effective amount of an ophthalmic pharmaceutical composition of claim 1 to the affected eye of a human or other mammal in need thereof.
10. The method of claim 9 wherein said applying comprises applying 1 to 2 drops of a composition comprising from about 0.01 percent weight/volume to about 5 percent weight/volume of compound (I) 1 to 4 times daily.
11. The method of claim 9 wherein said composition comprises a plurality of glaucoma treatment agents.
12. The method of claim 11 wherein at least one glaucoma treatment agent is selected from the group consisting of:
β-blockers, prostaglandin analog, carbonic anhydrase inhibitors, α2 agonists, miotics, rho kinase inhibitors, serotonergic agonists, and neuroprotectants.