Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/3277
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dc.contributor.authorShah, Amisha S.-
dc.date.accessioned2012-05-22T06:59:53Z-
dc.date.available2012-05-22T06:59:53Z-
dc.date.issued2012-
dc.identifier.urihttp://10.1.7.181:1900/jspui/123456789/3277-
dc.description.abstractThe purpose of this study was to work out a method of compression of floating pellets. It was assumed that this form should reside in the stomach floating for several hours and gradually release the drug in a controlled way. Compression of pellets into tablets, being a modern technological process, is much more perfect than enclosing them in a hard gelatin capsule.Pellets were prepared by wet granulation of powder mixture, spheronization of the granulated mass followed by drying. Two kinds of diluent, Avicel PH102 and lactose, HPMC K100M and sodium hydrocarbonate were the main components of pellet core. The process and formulation parameters for the pellet formulation were optimized by using 23 full factorial design.The best formulation was selected based on the criteria like controlled drug release for 24 hrs., Optimum floating time and Sphericity. The best was was then compressed into a tablet using cealose as a cushioning agent. The drug release profile of the compressed pellets was found to be same as that of non-compressed pellets. Thus it was concluded that pellets were compressed properly without any damage to the core.en_US
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPDR00163en_US
dc.subjectDissertation Reporten_US
dc.subjectPharmacrutical Technologyen_US
dc.subject10MPHen_US
dc.subject10MPH101en_US
dc.subjectPDR00163en_US
dc.titleDesign Development and Optimization of Floating Pelletsen_US
dc.typeDissertationen_US
Appears in Collections:M.Pharm. Research Reports, Department of Pharmaceutical Technology and Biopharmaceutics

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