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Please use this identifier to cite or link to this item: http://172.20.40.131:8080/jspui/handle/123456789/343
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dc.contributor.authorAundhia, Chintan-
dc.contributor.authorSeth, Avinash-
dc.contributor.authorChauhan, Sachin-
dc.contributor.authorShah, Nirmal-
dc.contributor.authorJavia, Ankur-
dc.date.accessioned2019-07-23T07:39:56Z-
dc.date.available2019-07-23T07:39:56Z-
dc.date.issued2015-
dc.identifier.issn2249-3387-
dc.identifier.urihttp://localhost:80/xmlui/handle/123456789/343-
dc.description.abstractThe present research work focuses on improving the bioavailability of the anti osteoporotic drug Risedronate Sodium. This drug belongs to BCS class III which implies that it is permeability rate limited. Hence an attempt was made to reduce the particle size to nano dimensions using ionotropic gelation technique. In this technique, chitosan was used as the polymer and sodium Tri poly Phosphate was used as the cross linking agent. The resulting nanoparticles were optimized using 32 full factorial design and characterized for their entrapment efficiency, percent yield, in vitro diffusion studies. The particle size and zeta potential was found out and surface morphology was studied using Scanning electron microscopy. The in vivo studies clearly showed a marked improvement in the bioavailability of the nanoparticles as compared to the plain drug suspension.en_US
dc.language.isoen_USen_US
dc.publisherAmerican Journal of Pharmtech Researchen_US
dc.subjectRisedronate Sodiumen_US
dc.subjectNanoparticlesen_US
dc.subjectBioavailabilityen_US
dc.titleBioavailability Enhancement of Risedronate Sodium by Formulation of Nanoparticles for Treatment of Osteoporosisen_US
dc.typeArticleen_US
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