PH SENSITIVE HYDROGELS OF LEVOFLOXACIN HEMIHYDRATE FOR OPHTHALMIC DRUG DELIVERY
Prachi Saxena*, Swatantra K. S. Kushwaha
Abstract
To achieve effective ophthalmic therapy, an adequate amount of active
ingredient must be delivered and maintained within the eye. The most
frequently used dosage forms i.e., eye solutions, eye ointments, eye
gels and eye suspensions are compromised in their effectiveness by
several limitations leading to poor ocular bioavailability. Stimuli
sensitive hydrogels are of very importance in this regard, they undergo
reversible volume and/or sol-gel phase transitions in response to
physiological (temperature, pH and presence of ions in organism
fluids, enzyme substrate) or other external (electric current, light)
stimuli. They help to increase in precorneal residence time of drug to a sufficient extent that
an ocularly delivered drug can exhibit its maximum biological action. The present work
describes the formulation and evaluation of pH sensitive ophthalmic Hydrogels of an
Antibacterial agent, “Levofloxacin hemihydrate”. “Levofloxacin” is a widely used drug for
treatment of acute conjunctivitis. However Conventional ophthalmic dosage forms of
Levofloxacin generally suffer the drawbacks of poor bioavailability due to its pH dependent
solubility. To increase the solubility of Levofloxacin, the pH Sensitive ophthalmic hydrogels
of the drug were formulated along with β-Cyclodextrin. Carbopol 940 was used as the gelling
agent in combination with Hydroxypropylmethylcellulose (+3000cps) which acted as a
viscosity enhancing agent. The developed formulation was therapeutically efficacious, stable,
and non-irritant and provided sustained release of the drug over a 6-h period. The developed
system is thus a viable alternative to conventional eye drops.
Keywords: Ophthalmic; pH sensitive; hydrogel; Levofloxacin; instillation; viscosity
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