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dc.contributor.authorMaru, S M
dc.date.accessioned2013-05-26T10:28:53Z
dc.date.available2013-05-26T10:28:53Z
dc.date.issued2005
dc.identifier.citationThe East and Central African Journal of Pharmaceutical Sciences Vol. 8 (3) 2005: pp 62-66en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/25935
dc.description.abstractThis study aimed at investigating the influence of varying proportions of the surfactant span 60, cholesterol and dicetylphosphate on the morphology, particle size distribution, entrapment efficiency and in vitro drug release of encapsulated tenoxicam niosomes. In vitro stability studies of the niosomes were then performed using blood from albino rats. Drug release from the niosomes showed biphasic sustained release pattern of tenoxicam for a period of 24 h. The results obtained show that niosomes of tenoxicam can be prepared as carriers for transdermal therapyen
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.subjectNiosomes, Tenoxicam, Cholesterol, Span 60, Dicetyl phosphateen
dc.titleFormulation and Evaluation of Tenoxicam Niosomesen
dc.typeArticleen
local.publisherDepartment of Pharmaceutics and Pharmacy Practiceen


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