Ophthalmic formulation with novel gum composition
There is provided a pharmaceutical composition suitable for topical administration to an eye, the composition comprising (a) a pharmacologically effective concentration of an active agent and (b) a combination of at least two ophthalmically compatible polymers comprising a novel gum system. In preferred embodiments of the present invention, the compositions increase the retention time of the active agent in the eye, when compared to compositions with other gums or gum systems.
1. A pharmaceutical composition suitable for topical administration to an eye, comprising: (a) a pharmacologically effective concentration of an active agent; and (b) a set of at least two ophthalmically compatible polymers selected from the group consisting of konjac and sodium alginate; konjac and hydroxy propyl guar; konjac and propylene glycol alginate; konjac and Carbopol 971; hydroxy propyl guar and agarose; propylene glycol alginate and agarose; and propylene glycol alginate and scleroglucan.
2. The pharmaceutical composition of claim 1 , wherein the active agent is a steroid.
3. The pharmaceutical composition of claim 1 wherein the active agent is an NSAIDS compound.
4. The pharmaceutical composition of claim 1 , wherein the active agent is an oxazolidinone antibiotic drug.
5. The pharmaceutical composition of claim 4 wherein the oxazolidinone antibiotic drug of a compound of formula (I): wherein: R 1 is selected from (a) H, (b) C 1-8 alkyl optionally substituted with at least one F, Cl, OH, C 1-8 alkoxy, and C 1-8 acyloxy or C 1-8 benzoxy, including a C 3-6 cycloalkyl group, (c) amino, (d) mono- and di(C 1-8 alkyl)amino and (e) C 1-8 alkoxy groups; R 2 and R 3 are independently selected from H, F and Cl groups; R 4 is H or CH 3 ; R 5 is selected from H, CH 3 , CN, CO 2 R 1 and (CH 2 ) m R 6 groups, where R 1 is as defined above, R 6 is selected from H, OH, OR 1 , OCOR 1 , NHCOR 1 , amino, mono- and di(C 1-8 alkyl)amino groups, and m is 1 or 2; n is 0, 1 or 2; and X is O, S, SO, SO 2 , SNR 7 or S(O)NR 7 where R 7 is seleceted from H, C 1-4 alkyl (optionally substituted with one or more F, Cl, OH, C 1-8 alkoxy, amino, C 1-8 mono- or di(C 1-8 alkyl)amino groups), and p-toluenesulfonyl groups; or a pharmaceutically acceptable salt thereof.
6. The pharmaceutical composition of claim 5 wherein, in formula (I), R 1 is CH 3 ; R 2 and R 3 are independently selected from H and F but at least one of R 2 and R 3 is F; R 4 and R 5 are each H; n is 1; and X is selected from O, S and SO 2.
7. The pharmaceutical composition of claim 4 wherein the oxazolidinone antibiotic drug is selected from the group consisting of: linezolid, eperezolid, N-((5S)-3-(3-fluoro-4-(4-(2-fluoroethyl)-3-oxopiperazin-1-yl)phenyl)-2-ox-ooxazolidin-5-ylmethyl-acetamide, (S)—N-[[3-[5-(3-pyridyl)thiomorphen-2-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide, (S)—N-[[3-[5-(4-pyridyl)pyrid-2-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide hydrochloride and N-[[(5S)-3-[4-(1,1-dioxido-4-thiomorpholiny)-3,5-difluorophenyl]-2-oxo-5-oxazoldinyl]methyl]acetamide.
8. The pharmaceutical composition of claim 4 wherein the oxazolidinone antimicrobial drug is linezolid.
9. The pharmaceutical composition of claim 1 , further comprising a cyclodextrin compound in a concentration sufficient to ensure that essentially all of the active agent in the composition is in solution.
10. The pharmaceutical composition of claim 9 wherein the cyclodextrin compound is selected from the group consisting of α-cyclodextrin, β-cyclodextrin, γ-cyclodextrin, an alkylcyclodextrin, a hydroxyalkylcyclodextrin, a carboxyalkyl-cyclodextrin, and sulfoalkylether cyclodextrin.
11. The pharmaceutical composition of claim 9 wherein the cyclodextrin compound is selected from the group consisting of hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin.
12. The pharmaceutical composition of claim 9 wherein the cyclodextrin concentration is about 1 mg/ml to about 500 mg/ml.
13. The pharmaceutical composition of claim 1 , wherein the set of at least two ophthalmically compatible polymers reduces the rate of removal of the composition from the eye by lacrimation, such that a concentration of the active agent in lacrimal fluid of the eye is maintained above the MIC 90 for at least about 2 hours following topical application to the eye.
14. A method of treating and/or preventing a disease or infection in a an eye of a warm-blooded subject, the method comprising administering to the eye of the subject a therapeutically or prophylactically effective amount of the composition of claim 1 .
15. A method of use of a composition of claim 1 in manufacture of a medicament for topically treating or preventing a disease or infection of an eye of a warm-blooded subject.
16. A pharmaceutical composition suitable for topical administration to an eye, comprising: (a) an oxazolidinone antimicrobial drug in a concentration effective for treatment and/or prophylaxis of a gram-positive bacterial infection of at least one tissue of the eye; (b) a pharmaceutically acceptable cyclodextrin compound in a cyclodextrin concentration sufficient to maintain the linezolid in solution; and (c) a set of at least two ophthalmically compatible polymers selected from the group consisting of konjac and sodium alginate; konjac and hydroxy propyl guar; konjac and propylene glycol alginate; konjac and Carbopol 971; hydroxy propyl guar and agarose; propylene glycol alginate and agarose; and propylene glycol alginate and scleroglucan.
17. The pharmaceutical composition of claim 16 wherein the oxazolidinone antibiotic drug of a compound of formula (I): 3wherein: R 1 is selected from (a) H, (b) C 1-8 alkyl optionally substituted with at least one F, Cl, OH, C 1-8 alkoxy, and C 1-8 acyloxy or C 1-8 benzoxy, including a C 3-6 cycloalkyl group, (c) amino, (d) mono- and di(C 1-8 alkyl)amino and (e) C 1-8 alkoxy groups; R 2 and R 3 are independently selected from H, F and Cl groups; R 4 is H or CH 3 ; R 5 is selected from H, CH 3 , CN, CO 2 R 1 and (CH 2 ) m R 6 groups, where R 1 is as defined above, R 6 is selected from H, OH, OR 1 , OCOR 1 , NHCOR 1 , amino, mono- and di(C 1-8 alkyl)amino groups, and m is 1 or 2; n is 0, 1 or 2; and X is O, S, SO, SO 2 , SNR 7 or S(O)NR 7 where R 7 is selected from H, C 1-4 alkyl (optionally substituted with one or more F, Cl, OH, C 1-8 alkoxy, amino, C 1-8 mono- or di(C 1-8 alkyl)amino groups), and p-toluenesulfonyl groups; or a pharmaceutically acceptable salt thereof.
18. The pharmaceutical composition of claim 17 wherein, in formula (I), R 1 is CH 3 ; R 2 and R 3 are independently selected from H and F but at least one of R 2 and R 3 is F; R 4 R 5 each H; n is 1; and X is selected from O, S and SO 2.
19. The pharmaceutical composition of claim 17 wherein the oxazolidinone antibiotic drug is selected from the group consisting of: linezolid, eperezolid, N-((5S)-3-(3-fluoro-4-(4-(2-fluoroethyl)-3-oxopiperazin-1-yl)phenyl)-2-ox-ooxazolidin-5-ylmethyl)-acetamide, (S)—N-[[3-[5-(3-pyridyl)thiophen-2-yl]-2-oxo-5-oxazolidinyl]methy]acetamide,(S)—N-[[3-[5-(4-pyridyl)pyrid-2-yl]-2-oxo-5-oxazolidinyl]methyl]acetamide hydrochloride and N-[[(5S)-3-[4-(1,1-dioxido-4-thiomorpholiny)-3,5-difluorophenyl]-2-oxo-5-oxazoldinyl]methyl]acetamide.
20. The pharmaceutical composition of claim 17 wherein the oxazolidinone antimicrobial drug is linezolid.
21. The pharmaceutical composition of claim 20 , wherein the linezolid concentration is about 0.01 mg/ml to about 100 mg/ml.
22. The pharmaceutical composition of claim 16 wherein the cyclodextrin compound is selected from the group consisting of β-cyclodextrin, β-cyclodextrin, β-cyciodextrin, an alkylcyclodextrin, a hydroxyalkylcyclodextrin, a carboxyalkylcyclodextrin, and sulfoalkylether cyclodextrin.
23. The pharmaceutical composition of claim 16 wherein the cyclodextrin compound is selected from the group consisting of hydroxypropyl-β-cyclodextrin and sulfobutylether-β-cyclodextrin.
24. The pharmaceutical composition of claim 16 wherein the cyclodextrin compound is present at a concentration of about 1 mg/ml to about 500 mg/ml.