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dc.contributor.authorHargoli, S
dc.contributor.authorFarid, J
dc.contributor.authorAzarmi, SH
dc.contributor.authorGhanbarzadeh, S
dc.contributor.authorZakeri-Milani, P
dc.date.accessioned2018-08-26T08:03:34Z
dc.date.available2018-08-26T08:03:34Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49273
dc.description.abstractThe aim of this work was to develop the best formulations for naproxen suppositories. The effects of different bases and surfactants on the physicochemical characteristics of the suppositories were determined by several tests such as weight variation, melting point, assay, hardness, and release rate. All formulations met the standard criteria for tested physicochemical parameters; weight variation (97-112%), content uniformity (97-105%), melting point (4.66-8.7 min) and hardness tests (>5400 g). Based on release rate studies, hydrophilic, and lipophilic bases without surfactants were not suitable bases for naproxen suppository. Amongst the formulations containing surfactants only Witepsol H15 with 0.5% w/w of Tween 80 and Witepsol W35 with 0.5% of cetylpyridinium chloride were suitable and released nearly complete drug during 30 and 60 min, respectively. This study demonstrates the effects of incorporation of known agents on the in vitro release characteristics of naproxen suppository.
dc.language.isoEnglish
dc.relation.ispartofINDIAN JOURNAL OF PHARMACEUTICAL SCIENCES
dc.subjectNaproxen
dc.subjectpolyethylene glycols
dc.subjectsuppository
dc.subjectsurfactant
dc.subjectWitepsol
dc.titlePreparation and In Vitro Evaluation of Naproxen Suppositories
dc.typeArticle
dc.citation.volume75
dc.citation.issue2
dc.citation.spage143
dc.citation.epage148
dc.citation.indexWeb of science
dc.identifier.DOIDOI: 10.4103/0250-474X.115458
dc.citation.URLhttps://www.ijpsonline.com/articles/preparation-and-iin-vitroi-evaluation-of-naproxen-suppositories.html


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