Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/37465
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dc.coverage.spatialPHARMACYen_US
dc.date.accessioned2015-03-17T07:58:21Z-
dc.date.available2015-03-17T07:58:21Z-
dc.date.issued2015-03-17-
dc.identifier.urihttp://hdl.handle.net/10603/37465-
dc.description.abstractThe most important property of a drug delivery system is its ability to deliver the active pharmaceutical ingredient API to the site of action in the body in an amount sufficient to produce the desired therapeutic response This property of the drug delivery system is referred to as bioavailability Bioavailability is more precisely defined as the rate and extent of absorption availability of drug to the systemic circulation About 95percentage of all new potential therapeutics API exhibit low and variable oral bioavailability due to their poor aqueous solubility at physiological pHs and consequent low dissolution rate These drugs are classified as class II drugs under BCS and pose challenging problems in their pharmaceutical product development process The drug in solid dosage form tablet must undergo dissolution before it is available for absorption from gastrointestinal tract Dissolution forms the rate limiting step in the absorption of drugs from solid dosage forms especially when the drug is poorly soluble newline newline newlineen_US
dc.format.extent1-257en_US
dc.languageEnglishen_US
dc.relationNOS.1-104en_US
dc.rightsuniversityen_US
dc.titleFACTORIAL STUDIES ON ENHANCEMENT OF SOLUBILITY DISSOLUTION RATE BIOAVAILABILITY AND FORMULATION DEVELOPMENT OF SELECTED BCS CLASS II DRUGS ETORICOXIB AND ACECLOFENACen_US
dc.title.alternativeen_US
dc.creator.researcherGOPINATH Sen_US
dc.subject.keywordBIOAVAILABILITYen_US
dc.subject.keywordDEVELOPMENT OF SELECTED BCS CLASSen_US
dc.subject.keywordDRUGS ETORICOXIB AND ACECLOFENACen_US
dc.subject.keywordENHANCEMENT OF SOLUBILITYen_US
dc.description.noteReference pgs: 92-100 Summary pgs: 257en_US
dc.contributor.guideCHOWDARY KPR DRen_US
dc.publisher.placeChennaien_US
dc.publisher.universitySri Ramachandra Universityen_US
dc.publisher.institutionCollege of Pharmacyen_US
dc.date.registered01/04/2008en_US
dc.date.completed17/02/2015en_US
dc.date.awarded17/02/2015en_US
dc.format.dimensions-en_US
dc.format.accompanyingmaterialNoneen_US
dc.source.universityUniversityen_US
dc.type.degreePh.D.en_US
Appears in Departments:College of Pharmacy

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10 chapter - ii.pdfAttached File241.7 kBAdobe PDFView/Open
11 chapter - iii.pdf654.32 kBAdobe PDFView/Open
12 chapter - iv.pdf424.08 kBAdobe PDFView/Open
13 chapter - v.pdf506.06 kBAdobe PDFView/Open
14 chapter - vi.pdf1.47 MBAdobe PDFView/Open
15 chapter - vii.pdf586.04 kBAdobe PDFView/Open
16 chapter - viii.pdf384.39 kBAdobe PDFView/Open
17 chapter - ix.pdf277.93 kBAdobe PDFView/Open
18 chapter - x.pdf305.85 kBAdobe PDFView/Open
1 front page.pdf77.67 kBAdobe PDFView/Open
2 declaration.pdf8.92 kBAdobe PDFView/Open
3 certificate.pdf8.69 kBAdobe PDFView/Open
4 acknowledgement.pdf127.37 kBAdobe PDFView/Open
5 list of tables.pdf114.51 kBAdobe PDFView/Open
6 list of figures.pdf179.64 kBAdobe PDFView/Open
7 list of abbreviations.pdf160.75 kBAdobe PDFView/Open
8 contents.pdf184.02 kBAdobe PDFView/Open
9 chapter - i.pdf233 kBAdobe PDFView/Open


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