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dc.contributor.authorYazan, Y
dc.contributor.authorÖzer, AY
dc.contributor.authorErol, K
dc.date.accessioned2019-10-18T19:02:32Z
dc.date.available2019-10-18T19:02:32Z
dc.date.issued1996
dc.identifier.issn0363-9045
dc.identifier.urihttps://dx.doi.org/10.3109/03639049609058573
dc.identifier.urihttps://hdl.handle.net/11421/10659
dc.descriptionWOS: A1996TY63300013en_US
dc.description.abstractThe nasal route has been shown to be effective for the administration of numerous drugs in order to improve drug bioavailability. A nasal gel of verapamil hydrochloride was formulated and evaluated pharmacodynamically in humans, using electrocardiographic results, with comparison to oral and IV routes. Seven volunteers were involved in the study and the pharmacodynamic parameters were evaluated statistically. Experimental nasal gel showed similar pharmacodynamic results with the intravenous route, which is a hint to the reduction in verapamil-induced first-pass metabolism. However, oral route of administration showed a tendency of less efficacy. No reasonable effect of verapamil could be obtained with the placebo group.en_US
dc.language.isoengen_US
dc.publisherMarcel Dekker Incen_US
dc.relation.isversionof10.3109/03639049609058573en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titlePharmacodynamic comparison of a nasal formulation of verapamil and intravenous and oral dosage formsen_US
dc.typearticleen_US
dc.relation.journalDrug Development and Industrial Pharmacyen_US
dc.contributor.departmentAnadolu Üniversitesien_US
dc.identifier.volume22en_US
dc.identifier.issue3en_US
dc.identifier.startpage281en_US
dc.identifier.endpage284en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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