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dc.contributor.authorBrown, Chandra Demona
dc.date.accessioned2014-03-05T16:03:45Z
dc.date.available2014-03-05T16:03:45Z
dc.date.issued2002-08
dc.identifier.otherbrown_chandra_d_200208_ms
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/brown_chandra_d_200208_ms
dc.identifier.urihttp://hdl.handle.net/10724/29500
dc.description.abstractSeveral methods for removing samples from finished semisolid dosage forms are in current use. Sampling methods for semisolids vary among industry, but no standard method exists. These methods are tailored to specific formulations and manufacturers. This creates the possibility for differences in the determination of in vitro release specification, batch variability and stability profiles. The present study evaluates a standard method that will minimize variability in sampling, which will enhance the performance testing of semisolids.
dc.languageA method of sampling a finished semisolid dosage form
dc.publisheruga
dc.rightspublic
dc.subjectHydrocortisone
dc.subjectFinished Semisolid
dc.subjectSampling method
dc.subjectHPLC
dc.titleA method of sampling a finished semisolid dosage form
dc.typeThesis
dc.description.degreeMS
dc.description.departmentCollege of Pharmacy
dc.description.majorPharmacy
dc.description.advisorAnthony Capomacchia
dc.description.committeeAnthony Capomacchia
dc.description.committeeStuart Feldman
dc.description.committeePhillip Greenspan


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