dc.contributor.author | Behnam, B | |
dc.contributor.author | Rezazadehkermani, M | |
dc.contributor.author | Ahmadzadeh, S | |
dc.contributor.author | Mokhtarzadeh, A | |
dc.contributor.author | Nematollahi-Mahani, SN | |
dc.contributor.author | Pardakhty, A | |
dc.date.accessioned | 2018-08-26T07:12:58Z | |
dc.date.available | 2018-08-26T07:12:58Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44850 | |
dc.description.abstract | The 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.iso | English | |
dc.relation.ispartof | ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY | |
dc.subject | Doxorubicin | |
dc.subject | niosome | |
dc.subject | magnetite nanoparticles | |
dc.subject | intraperitoneal chemotherapy | |
dc.subject | cytotoxicity | |
dc.title | Microniosomes for concurrent doxorubicin and iron oxide nanoparticles loading; preparation, characterization and cytotoxicity studies | |
dc.type | Article | |
dc.citation.volume | 46 | |
dc.citation.issue | 1 | |
dc.citation.spage | 118 | |
dc.citation.epage | 125 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.1080/21691401.2017.1296850 | |