We claim:
1. A pharmaceutical composition suitable for ophthalmic use comprising 0.005% w/v latanoprost or a pharmaceutically acceptable salt therof, 0.15% w/v castor oil, 0.2 to 0.75% w/v of polyethylene glycol hydroxystearate, a co-solvent, a chelating agent, a preservative, and pharmaceutically acceptable vehicle,
wherein the ratio of oil to polyethylene glycol hydroxystearate is less than 1.0,
wherein the composition is in the form of a self-emulsifying micro-emulsion with average droplet size of about 100 nm or less and a zeta potential between −0.1 mV to −20 mV,
wherein the composition does not comprise a cationic surfactant, and
wherein the composition does not comprise a quaternary ammonium compound.
2. The pharmaceutical composition as claimed in claim 1 Wherein the emulsion has an average droplet size of less than 100 nanometers in diameter.
3. The pharmaceutical composition as claimed in claim 2 , wherein the emulsion has a percent transmission greater than 70%.
4. The pharmaceutical composition as claimed in claim 2 , wherein the emulsion has a percent transmission greater than 80%.
5. The pharmaceutical composition as claimed in claim 1 wherein the composition does not show any clinical sign of ocular irritation when tested in rabbits.