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dc.contributor.authorPatel, Viralkumar
dc.contributor.authorPatel, Natavarlal M.
dc.date.accessioned2014-04-15T08:00:21Z
dc.date.available2014-04-15T08:00:21Z
dc.date.issued2007-09
dc.identifier.citationPatel , V & Patel , N M 2007 , ' Statistical evaluation of influence of viscosity and content of polymer on dipyridamole release from floating matrix tablets: a technical note ' , AAPS PharmSciTech , vol. 8 , no. 3 , pp. E140-E144 . https://doi.org/10.1208/pt0803069
dc.identifier.issn1522-1059
dc.identifier.otherPURE: 308511
dc.identifier.otherPURE UUID: 4107b12e-c1ba-4f2d-8797-433a3a343e03
dc.identifier.otherPubMed: 17915819
dc.identifier.otherScopus: 34548538082
dc.identifier.urihttp://hdl.handle.net/2299/13359
dc.description.abstractThe present investigation described the influence of viscosity and content of HPMC on dipyridamole release using 32 full factorial design. All formulations had desired floating lag time (<2 minutes) regardless of viscosity and content of polymeric matrices. Results of multiple regression analysis indicate that both factors significantly affect the diffusion exponent (n), release rate constant (k), and percentage drug release at 1 hour, 4 hours, 6 hours, and 12 hour, (P<.05). Mechanism of drug release was found to be anomalous type to case-II transport depending upon the viscosity and content of polymer. It was found that content of HPMC had a dominant role in the initial phase of drug release, while in the later phase viscosity of HPMC Predominateden
dc.language.isoeng
dc.relation.ispartofAAPS PharmSciTech
dc.subjectDiffusion
dc.subjectDipyridamole
dc.subjectMethylcellulose
dc.subjectRegression Analysis
dc.subjectSolubility
dc.subjectTablets
dc.subjectViscosity
dc.titleStatistical evaluation of influence of viscosity and content of polymer on dipyridamole release from floating matrix tablets: a technical noteen
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionPharmaceutics
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionBioadhesive Drug Delivery Group
dc.contributor.institutionPharmaceutical Analysis and Product Characterisation
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.description.statusPeer reviewed
rioxxterms.versionofrecordhttps://doi.org/10.1208/pt0803069
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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