Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/337441
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dc.coverage.spatial
dc.date.accessioned2021-08-24T04:42:16Z-
dc.date.available2021-08-24T04:42:16Z-
dc.identifier.urihttp://hdl.handle.net/10603/337441-
dc.description.abstractBackground: Lovastatin (LVS); HMG CoA inhibitor, is a drug of choice for newlinehyperlipidemia. Its clinical efficacy is limited due to its low aqueous solubility, incomplete absorption, short-half life, first pass metabolism, low bioavailability, and adverse effects newlineetc. newlineObjective: The objective of the present study was to improve the solubility of Lovastatin newlineand develop mucoadhesive film of solid dispersions for buccal delivery to enhance newlinebioavailability. newline
dc.format.extent
dc.languageEnglish
dc.relation
dc.rightsuniversity
dc.titleSolubility enhancement system design for transbuccal delivery In vitro characterization and Invivo evaluation of lovastatin
dc.title.alternative
dc.creator.researcherBhuvaneshwari R. Sharannavar
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.description.noteLovastatin, PEG 4000, PVPK30, Solid dispersion, HPMCK4M, HPMC E5LV, chitosan, Ex-vivo bioadhesion, ex-vivo permeation, bioavailability
dc.contributor.guideSunil Satyappa Jalalpure
dc.publisher.placeBelgaum
dc.publisher.universityKLE University
dc.publisher.institutionFaculty of Pharmacy
dc.date.registered
dc.date.completed2020
dc.date.awarded
dc.format.dimensions
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Pharmacy

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