Search Results - "Mokale, Vinod J."
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Enhanced solubility and bioavailability of lovastatin using stabilized form of self-emulsifying drug delivery system
Published in Colloids and surfaces. A, Physicochemical and engineering aspects (01-09-2015)“…•The present study deals with the development of stabilized self-emulsifying drug delivery system in the form of hydrogel.•Sodium alginate and HPMC were used…”
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High performance visible light photocatalysis of electrospun PAN/ZnO hybrid nanofibers
Published in Journal of industrial and engineering chemistry (Seoul, Korea) (25-09-2019)“…[Display omitted] •Fabrication of PAN/ZnO hybrid nanofibers using electrospinning technique at room temperature.•Uniform, well defined and bead free smooth…”
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Design, Synthesis and Evaluation of Antiinflammatory, Analgesic and Ulcerogenicity studies of Novel S-Substituted phenacyl-1,3,4-oxadiazole-2-thiol and Schiff bases of Diclofenac acid as Nonulcerogenic Derivatives
Published in Bioorganic & medicinal chemistry (15-02-2008)“…Diclofenac sodium is being used for its anti-inflammatory actions since 28 years, but as all the NSAIDs are suffering from the deadlier GI toxicities,…”
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Synthesis and pharmacological evaluation of novel 1-(2-(benzoyl-substituted-2-phenyl-1H-indol-5-carbony) hydrazinyloxy) vinyl nitrate derivatives as potent non-ulcerogenic, analgesic and anti-inflammatory agents
Published in Medicinal chemistry (Shp-sariqah, United Arab Emirates) (01-07-2010)“…Six derivatives of 1-(2-(benzoyl-(substituted)-2-phenyl-1H-indole-5-carbony) hydrazinyloxy) vinyl nitrate were synthesized and tested in vivo for…”
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Sodium alginate/HPMC/liquid paraffin emulsified (o/w) gel beads, by factorial design approach; and in vitro analysis
Published in Journal of sol-gel science and technology (01-07-2014)“…The present study involved development of a novel sodium alginate (SA)/HPMC/light liquid paraffin emulsified (o/w) gel beads containing Diclofenac sodium (DS)…”
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Formulation and optimisation of famotidine proniosomes: an in vitro and ex vivo study
Published in Journal of experimental nanoscience (22-01-2016)“…The aim of the study was to develop a proniosomal system for famotidine (FAM), a potent H 2 receptor antagonist that could efficiently deliver entrapped drug…”
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