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dc.contributor.authorYazan, Yasemin
dc.contributor.authorErol, K.
dc.date.accessioned2019-10-19T16:02:43Z
dc.date.available2019-10-19T16:02:43Z
dc.date.issued1990
dc.identifier.issn0363-9045
dc.identifier.urihttps://dx.doi.org/10.3109/03639049009025792
dc.identifier.urihttps://hdl.handle.net/11421/13888
dc.description.abstractThe bioavailabilities of single 100-mg oral and rectal doses of diphenylhydantoin sodium were studied in five healthy volunteers. The rectal form used was prepared at laboratory conditions and the oral form was a commercial preparation. Blood samples were analysed over a 72-hr period. Evaluation of the AUC, tmax and Cmax values have shown that the total absorption after the two routes of administration was the same while the Cmax and tmax differeden_US
dc.language.isoengen_US
dc.publisherInforma Healthcareen_US
dc.relation.isversionof10.3109/03639049009025792en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleComparison of the bioavailability of oral and rectal forms of diphenylhydantoin sodiumen_US
dc.typearticleen_US
dc.relation.journalDrug Development and Industrial Pharmacyen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Teknoloji Anabilim Dalıen_US
dc.identifier.volume16en_US
dc.identifier.issue11en_US
dc.identifier.startpage1849en_US
dc.identifier.endpage1856en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorYazan, Yasemin


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