Compositions for treatment of glaucoma

Abstract

Compositions for controlling glaucoma and ocular hypertension are disclosed.

Description

This invention is directed to compositions which are useful for the treatment of glaucoma and ocular hypertension.

BACKGROUND OF THE INVENTION

European Patent No. 253 717 discloses ophthalmic formulations containing combinations of specific beta adrenergic receptor antagonists (beta-blockers) and pilocarpine for the treatment of elevated intraocular pressure in patients refractory to treatment with beta-blockers alone. The patent discloses a beta-blocker concentration of 0.5 to 1.0 weight/volume percent (wt./v.%) and a pilocarpine concentration of 2 to 4 wt./v.%. The claimed formulation is made by combining lyophilized pilocarpine hydrochloride and a solution of an ophthalmic beta-blocker.

A product known as Normoglaucon has been sold in Germany. The product contains 2% pilocarpine and 0.1% metipranolol.

U.S. Pat. No. 4,474,751 discloses an ophthalmic drug delivery system using selected polymers which use the body temperature and pH to induce liquid to gel transition of the polymers. The patent discloses an extensive list of drugs which can be administered by the system, including a combination of timolol or R-timolol with pilocarpine. The specific examples do not describe any formulations of any drug combinations.

SUMMARY OF THE INVENTION

The present invention is directed to formulations for treating glaucoma and/or ocular hypertension in mammals, including humans. The formulations contain a combination of a beta-blocker, pilocarpine, a cation exchange resin, and a polyanionic polymer.

The invention is also directed to methods for treating glaucoma and/or ocular hypertension by topical administration of the formulations to the eye.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Many people suffering from glaucoma or ocular hypertension cannot control their elevated intraocular pressure (IOP) using beta-blockers alone. It is known that in many instances control can be gained by using an additional drug known to reduce intraocular pressure, such as pilocarpine, in combination with a beta-blocker. Pilocarpine is a cholinergic agonist that has been used for a long time to reduce intraocular pressure associated with glaucoma and ocular hypertension. While it is known to be relatively safe and effective, it does cause side effects, such as ocular discomfort, headache, and blurred vision. These side effects are uncomfortable for the patient and contribute to poor patient compliance. The present invention provides a formulation which is useful to those people requiring two drugs to control the elevated intraocular pressure associated with their glaucoma and/or ocular hypertension with a significant reduction in side effects.

The formulations of the present invention are believed to have the following advantages over known formulations: better patient compliance due to decreased side effects and by alleviating the need for two separate medications with different dosing regimens, better bioavailability of pilocarpine due to improved suspension properties, and reduced side effects.

The formulation of the present formulation contains about 0.1 to 1.0 weight/volume % (wt./vol. %) beta-blocker; about 0.25 to 10.0 wt./vol. % pilocarpine; about 0.05 to 10 wt./vol. % pharmaceutically acceptable ion exchange resin and about 0.01 to 5.0 wt./vol. % polyanionic polymer such as Carbomer 934P or 974P. Useful beta-blockers (e.g. betaxolol, timolol, befunolol, labetalol, propranolol, bupranolol, metaprolol, bunalol, esmalol, pindolol, carteolol, hepunolol, metipranolol, celiprolol, azotinolol, diacetolol, acebutolol, atenolol, isoxaprolol), polyanionic polymers, and ion exchange resins of the invention are disclosed in U.S. Pat. No. 4,911,920, from which this case descends, and which is incorporated herein by reference.

Since both pilocarpine and most beta-blockers are basic compounds, they readily bind with strongly acidic ion exchange resins, such as poly(styrene-divinyl benzene) sulfonic acid. Upon administration to the eye, the pilocarpine and beta-blocker relatively slowly disassociate from the resin. Although the beta-blocker, betaxolol, alone has been formulated with an ion exchange resin and a polyanionic polymer resulting in a more comfortable formulation (Betoptic.RTM. S, available from Alcon Laboratories, Inc.), it is unexpected that side effects associated with pilocarpine would be significantly reduced through use of the present formulation.

The stability of pilocarpine in solution is limited at physiological pH. Therefore, the formulations of the present invention are prepared in two parts. As shown in the examples, the pilocarpine portion (Part I) is prepared at or below about pH 5. The beta-blocker portion (Part II) is prepared at about pH 8. Mixing of the two parts by the patient, doctor, or pharmacist is required before application to the eye. The reconstituted formulation is close to physiological pH and is stable for about one month at room temperature.

The preferred reconstituted formulation contains 0.25% betaxolol base, 1.75% pilocarpine, 0.25% poly(styrene-divinyl benzene) sulfonic acid (Amberlite, Rohm & Haas), and 0.40% of Carbomer 934P (B.F. Goodrich). Betaxolol is a known compound, see U.S. Pat. Nos. 4,252,984, 4,311,708, and 4,342,783.

The formulations of the present invention can be used to control glaucoma and ocular hypertension through topical administration to the eye one to four times daily according to the discretion of a skilled clinician.

The following examples are representative of formulations of the present invention and are not meant to be limiting.

EXAMPLE 1

______________________________________INGREDIENTS PERCENT wt./vol.______________________________________PART 1 FORMULAPilocarpine Hydrochloride 8.75Sodium Hydroxide and/or QS pH to 5.0 +/- 0.2Hydrochloric AcidPurified Water QS to 100PART II FORMULABetaxolol Hydrochloride 0.35*Poly(Styrene-Divinyl Benzene) 0.313Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 934P 0.50Boric Acid 0.10Mannitol 2.20Disodium Edetate 0.0125Benzalkonium Chloride, Solution 0.0125 + 5% XSSodium Hydroxide and/or QS pH to 8.0 +/- 0.2Hydrochloric AcidPurified Water QS to 100______________________________________ *Equivalent to 0.313% Betaxolol Base

Reconstitution of Parts I and II

The product composition after reconstitution (1 mL of Part I, and 4 mL of Part II, is given below. The entire contents of Part I are transferred to the Part II container and mixed well for 60 seconds.

Reconstituted Product

______________________________________INGREDIENTS PERCENT wt./vol.______________________________________Betaxolol Hydrochloride, USP 0.28*Pilocarpine Hydrochloride, USP 1.75Poly(Styrene-Divinyl Benzene) 0.25Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 934P, NF 0.40Boric Acid, NF 0.08Mannitol, USP, USP 1.76Disodium Edetate, USP 0.01Benzalkonium Chloride, Solution, NF 0.01 + 5% XSPurified Water, USP 95-96______________________________________ *Equivalent to 0.25% Betaxolol Base

EXAMPLE 2

______________________________________INGREDIENTS PERCENT wt./vol.______________________________________PART 1 FORMULAPilocarpine Hydrochloride 8.75Sodium Hydroxide and/or QS pH to 5.0 +/- 0.2Hydrochloric AcidPurified Water QS to 100PART II FORMULABetaxolol Hydrochloride 0.35*Poly(Styrene-Divinyl Benzene) 0.313Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 974P 0.50Boric Acid 0.10Mannitol 2.20Disodium Edetate 0.0125Benzalkonium Chloride, Solution 0.0125 + 5% XSSodium Hydroxide and/or QS pH to 8.0 +/- 0.2Hydrochloric AcidHamposyl L 0.0375Purified Water QS to 100______________________________________ *Equivalent to 0.313% Betaxolol Base

Reconstitution of Parts I and II

The product composition after reconstitution (1 mL of Part I, and 4 mL of Part II, is given below. The entire contents of Part I are transferred to the Part II container and mixed well for 60 seconds.

______________________________________Reconstituted ProductINGREDIENTS PERCENT wt./vol.______________________________________Betaxolol Hydrochloride, USP 0.28*Pilocarpine Hydrochloride, USP 1.75Poly(Styrene-Divinyl Benzene) 0.25Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 974P, NF 0.40Boric Acid, NF 0.08Mannitol, USP, USP 1.76Disodium Edetate, USP 0.01Benzalkonium Chloride, Solution, NF 0.01 + 5% XSHamposyl L 0.03Purified Water, USP 95-96______________________________________ *Equivalent to 0.25% Betaxolol Base

EXAMPLE 3

Formulations containing different beta-blockers at different concentrations and different concentrations of pilocarpine can be made by a person skilled in the art of making ophthalmic formulations.

______________________________________INGREDIENTS PERCENT wt./vol.______________________________________PART 1 FORMULAPilocarpine Hydrochloride 1.25 to 50*Sodium Hydroxide and/or QS pH to 5.0 +/- 0.2Hydrochloric AcidPurified Water QS to 100PART II FORMULABeta-blocker 0.125 to 1.252**Poly(Styrene-Divinyl Benzene) 0.125 to 1.252Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 934P 0.50Boric Acid 0.10Mannitol 2.20Disodium Edetate 0.0125Benzalkonium Chloride, Solution 0.0125 + 5% XSSodium Hydroxide and/or QS pH to 8.0 +/- 0.2Hydrochloric AcidPurified Water QS to 100______________________________________ *Equivalent to provide for 0.25 to 10.0 wt./vol. % upon reconstitution. **Equivalent to provide for 0.1 to 1.0 wt./vol. % upon reconstitution.

Reconstitution of Parts I and II

The product composition after reconstitution (1 mL of Part I, and 4 mL of Part II, is given below. The entire contents of Part I are transferred to the Part II container and mixed well for 60 seconds.

______________________________________Reconstituted ProductINGREDIENTS PERCENT wt./vol.______________________________________Beta-blocker 0.1 to 1.0Pilocarpine Hydrochloride 0.25 to 10.0Poly(Styrene-Divinyl Benzene) 0.1 to 1.0Sulfonic Acid (Amberlite IRP-69Hydrogen Form)Carbomer 934P, NF 0.40Boric Acid, NF 0.08Mannitol, USP, USP 1.76Disodium Edetate, USP 0.01Benzalkonium Chloride, Solution, NF 0.01 + 5% XSPurified Water, USP 95-96______________________________________

Claims

1. A topical ophthalmic composition for controlling glaucoma and/or ocular hypertension comprising 0.1 to 1.0 wt./vol. % betaxolol, 0.25 to 10.0 wt./vol. % pilocarpine, 0.05 to 10.0 wt./vol. % poly(styrene-divinyl benzene) sulfonic acid, and 0.01 to 5.0 wt./vol. % polyanionic polymer selected from the group consisting of Carbomer 934P and Carbomer 974P.

2. The composition of claim 1 wherein the polyanionic polymer is Carbomer 934P.

3. The composition of claim 2 wherein the betaxolol concentration is 0.25%, the pilocarpine concentration is 1.75%, the resin concentration is 0.25%, and the Carbomer 934P concentration is 0.40%.

4. The composition of claim 1 wherein the polyanionic polymer is Carbomer 974P.

5. The composition of claim 4 wherein the betaxolol concentration is 0.25%, the pilocarpine concentration is 1.75%, the resin concentration is 0.25%, and the Carbomer 974P concentration is 0.40%.

6. A method for controlling intraocular pressure by topically applying to the eye a composition which comprises 0.1 to 1.0 wt./vol. % betatolol, 0.25 to 10.0 wt./vol. % pilocarpine, 0.05 to 10.0 wt./vol. % poly(styrene-divinyl benzene) sulfonic acid, and 0.01 to 5.0 wt./vol. % polyanionic polymer selected from the group consisting of Carbomer 934P and Carbomer 974P.

7. The method of claim 6 wherein the polyanionic polymer is Carbomer 934P.

8. The method of claim 7 wherein the betaxolol concentration is 0.25%, the pilocarpine concentration is 1.75%, the resin concentration is 0.25%, and the Carbomer 934P concentration is 0.40%.

9. The method of claim 6 wherein the polyanionic polymer is Carbomer 974P.

10. The method of claim 9 wherein the betaxolol concentration is 0.25%, the pilocarpine concentration is 1.75%, the resin concentration is 0.25%, and the Carbomer 974P concentration is 0.40%.