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dc.contributor.authorPatel, Viralkumar
dc.contributor.authorPatel, Natavarlal M
dc.date.accessioned2014-04-15T09:00:20Z
dc.date.available2014-04-15T09:00:20Z
dc.date.issued2006-03
dc.identifier.citationPatel , V & Patel , N M 2006 , ' Intragastric floating drug delivery system of cefuroxime axetil : in vitro evaluation ' AAPS PharmSciTech , vol. 7 , no. 1 , pp. E118-E124 . https://doi.org/10.1208/pt070117
dc.identifier.issn1522-1059
dc.identifier.otherPURE: 308584
dc.identifier.otherPURE UUID: d10cd84c-08be-4ec3-a87a-2cae998d169a
dc.identifier.otherPubMed: 16584147
dc.identifier.otherScopus: 33644837054
dc.identifier.urihttp://hdl.handle.net/2299/13363
dc.description.abstractThis investigation describes the development of an intragastric drug-delivery system for cefuroxime axetil. The 3(2) full factorial design was employed to evaluate contribution of hydroxypropyl methyl cellulose (HPMC) K4M/HPMC K100 LV ratio (polymer blend) and sodium lauryl sulfate (SLS) on drug release from HPMC matrices. Tablets were prepared using direct compression technique. Formulations were evaluated for in vitro buoyancy and drug release study using United States Pharmacopeia (USP) 24 paddle-type dissolution apparatus using 0.1N HCl as a dissolution medium. Multiple regression analysis was performed for factorial design batches to evaluate the response. All formulations had floating lag times below 2 minutes and constantly floated on dissolution medium for more than 8 hours. It was found that polymer blend and SLS significantly affect the time required for 50% of drug release, percentage drug release at 12 hours, release rate constant, and diffusion exponent (P <.05). Also linear relationships were obtained between the amount of HPMC K100 LV and diffusion exponent as well as release rate constant. Kinetic treatment to dissolution profiles revealed drug release ranges from anomalous transport to case 1 transport, which was mainly dependent on both the independent variables.en
dc.language.isoeng
dc.relation.ispartofAAPS PharmSciTech
dc.subjectAnti-Bacterial Agents
dc.subjectCefuroxime
dc.subjectChemistry, Pharmaceutical
dc.subjectDrug Delivery Systems
dc.subjectMethylcellulose
dc.subjectSodium Dodecyl Sulfate
dc.subjectSolubility
dc.subjectStomach
dc.subjectTablets
dc.titleIntragastric floating drug delivery system of cefuroxime axetil : in vitro evaluationen
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
dc.relation.schoolSchool of Life and Medical Sciences
rioxxterms.versionofrecordhttps://doi.org/10.1208/pt070117
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue
herts.rights.accesstyperestrictedAccess


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