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dc.contributor.authorBehnam, B
dc.contributor.authorRezazadehkermani, M
dc.contributor.authorAhmadzadeh, S
dc.contributor.authorMokhtarzadeh, A
dc.contributor.authorNematollahi-Mahani, SN
dc.contributor.authorPardakhty, A
dc.date.accessioned2018-08-26T07:12:58Z
dc.date.available2018-08-26T07:12:58Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44850
dc.description.abstractThe current work deals with developing a suitable drug delivery system of doxorubicin (DOX) for intraperitoneal chemotherapy using niosomes through formulating non-ionic surfactants consisting of Brij (TM) 52, span (TM) 60 and Solulan (TM) C24. Entrapping the magnetite nanoparticles in the hydrophilic parts of niosomes was accompanied with high-efficient DOX loading by the current novel remote-loading method. Cytotoxicity of the prepared formulations was evaluated in vitro against A549 and PC-12 cell lines using the colorimetric WST-1 assay test. The obtained results revealed that, the cytotoxicity of DOX increased up to 22% especially on A549 cells by the current delivery system.
dc.language.isoEnglish
dc.relation.ispartofARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
dc.subjectDoxorubicin
dc.subjectniosome
dc.subjectmagnetite nanoparticles
dc.subjectintraperitoneal chemotherapy
dc.subjectcytotoxicity
dc.titleMicroniosomes for concurrent doxorubicin and iron oxide nanoparticles loading; preparation, characterization and cytotoxicity studies
dc.typeArticle
dc.citation.volume46
dc.citation.issue1
dc.citation.spage118
dc.citation.epage125
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/21691401.2017.1296850


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