Features and properties of bimatoprost implant
| Alternative names | Bimatoprost SR; bimatoprost sustained-release implant; Durysta™ |
|---|---|
| Class | Amides; antiglaucomas; lipids; prostaglandins; small molecules |
| Mechanism of action | Prostaglandin F2α receptor agonist |
| Route of administration | Implantation |
| Pharmacodynamics | Acts to lower intraocular pressure by increasing outflow of aqueous humour through both the trabecular meshwork (conventional) and uveoscleral routes (unconventional) |
| Pharmacokinetics | Following administration of bimatoprost implant, the highest concentrations of bimatoprost plus the metabolite bimatoprost acid are found in the iris–ciliary body (based on a study in dogs); minimal systemic exposure |
| Most common adverse reactions | Conjunctival hyperaemia, foreign body sensation, eye pain, photophobia, conjunctival haemorrhage, dry eye, eye irritation, intraocular pressure increased, corneal endothelial cell loss, vision blurred, iritis, headache |
| ATC codes: | |
| WHO ATC code | S01E-E03 (Bimatoprost) |
| EphMRA ATC code | S1E (Miotics and Antiglaucoma Preparations) |
| Chemical name | (Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-5-phenyl-1-pentenyl]cyclopentyl]-N-ethyl-5-heptenamide |