Design and development of loteprednol etabonate nanodispersion for ophthalmic drug delivery
Keywords:
Loteprednol Etabonate (LE), Nanodispersion, Post-operative inflammation, OphthalmicAbstract
Postoperative inflammation after cataract surgery can prolong visual recovery time, increase the treatment burden and elevate the risk of poor visual outcomes. Corticosteroids are potent anti-inflammatory agents that have been used successfully for decades to treat ocular inflammation. However, the side effects associated with topical corticosteroids including increased intraocular pressure, risk of cataract formation after long-term use, and decreased resistance to infection are of major concerns. Amongst the available topical corticosteroids Loteprednol Etabonate (LE), an ester-based corticosteroid has been selected for studies. The aim of the present study was to develop Loteprednol etabonate loaded nanodispersion for treatment of steroid responsive inflammatory conditions of eye with objectives of reducing the frequency of administration and increasing the solubility of drug. Non-solvent method was used to formulate nanodispersion. The formulation was assessed for particle size and polydispersity index, drug content, surface morphology, isotonicity, test of sterility, in-vitro & ex-vivo release. Mean particle size and PI of optimized batch was found to be 50±10nm and PI 0.2±0.1. No microbial growth was observed in optimized formulation during sterility testing and the formulation was isotonic when compared with marketed formulation and plain blood cells.
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