J
J. K. Pandit
Researcher at Banaras Hindu University
Publications - 29
Citations - 1419
J. K. Pandit is an academic researcher from Banaras Hindu University. The author has contributed to research in topics: Gellan gum & Chitosan. The author has an hindex of 17, co-authored 29 publications receiving 1259 citations.
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Journal ArticleDOI
Polymeric nanoparticulate system: a potential approach for ocular drug delivery.
TL;DR: DNPs have been shown to be amenable to targeting of the drug to the site of action, leading to a decreases in the dose required and a decrease in side effects, which makes them a novel polymeric drug delivery device, which fulfils the requirements for ophthalmic application.
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Chitosan coated sodium alginate-chitosan nanoparticles loaded with 5-FU for ocular delivery: in vitro characterization and in vivo study in rabbit eye.
TL;DR: The enhanced mucoadhesiveness of CH-SA-CH DNPs results in higher bioavailability as compared to the uncoated nanoparticles, and Optimized formulation was found non-irritant and tolerable when tested by modified Draize test in rabbit eye.
Journal ArticleDOI
Formulation of controlled release gellan gum macro beads of amoxicillin
TL;DR: The gellan macro beads may be suitable for gastro retentive controlled delivery of amoxicillin, and the effect of drug loading, stirring time, polymer concentration, electrolyte concentration, curing time etc. influencing the preparation of thegellan gum macro beads and the drug release were investigated.
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In vitro release kinetics and bioavailability of gastroretentive cinnarizine hydrochloride tablet.
TL;DR: It was demonstrated that the floating tablet CNZ could be a 24-h sustained release formulation and the greater bioavailability of HP1 was due to its longer retention in the gastric environment of the test animal.
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Ion-activated in situ gelling systems for sustained ophthalmic delivery of ciprofloxacin hydrochloride.
J. Balasubramaniam,J. K. Pandit +1 more
TL;DR: The developed formulations of an ophthalmic delivery system of an antibacterial agent, CPH, based on the concept of ion-activated in situ gelation provided sustained release of the drug over an 8-hr period in vitro.