Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/5634
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dc.contributor.authorZeybek, Ayça-
dc.contributor.authorŞanlı Mohamed, Gülşah-
dc.contributor.authorAk, Güliz-
dc.contributor.authorYılmaz, Habibe-
dc.contributor.authorŞanlıer, Şenay H.-
dc.date.accessioned2017-05-29T13:09:14Z
dc.date.available2017-05-29T13:09:14Z
dc.date.issued2014-07
dc.identifier.citationZeybek, A., Şanlı Mohamed, G., Ak, G., Yılmaz, H., and Şanlıer, Ş.H. (2014). In vitro evaluation of doxorubicin-incorporated magnetic albumin nanospheres. Chemical Biology and Drug Design, 84(1), 108-115. doi:10.1111/cbdd.12300en_US
dc.identifier.issn1747-0277
dc.identifier.issn1747-0277-
dc.identifier.urihttps://doi.org/10.1111/cbdd.12300
dc.identifier.urihttp://hdl.handle.net/11147/5634
dc.description.abstractMagnetic albumin nanospheres that incorporate doxorubicin (M-DOX-BSA-NPs) were prepared previously by our research group to develop magnetically responsive drug carrier system. This nanocarrier was synthesized as a drug delivery system for targeted chemotherapy. In this work, cytotoxic effects of doxorubicin (DOX)-loaded/unloaded or magnetic/non-magnetic nanoparticles and free DOX against PC-3 cells and A549 cells were determined with the MTT test and the results were compared with each other. DOX-loaded magnetic albumin nanospheres (M-DOX-BSA-NPs) were found more cytotoxic than other formulations. The quantitative data obtained from flow cytometry analysis further verified the higher targeting and killing ability of M-DOX-BSA-NPs than free DOX on both of the cancer cell lines. Additionally, the results of cell cycle analysis have showed that M-DOX-BSA-NPs affected G1 and G2 phases. Finally, cell images were obtained using spin-disk confocal microscopy, and cellular uptake of M-DOX-BSA-NPs was visualized. The findings of this study suggest that M-DOX-BSA-NPs represent a potential doxorubicin delivery system for targeted drug transport into prostate and lung cancer cells. In this study, we found that M-DOX-BSA-NPs provide many advantages as targeted drug delivery, enhanced drug killing ability and bioavailability based on cytotoxicity, flow cytometry, and confocal microscopy image results.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Inc.en_US
dc.relation.ispartofChemical Biology and Drug Designen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectA549 cell lineen_US
dc.subjectApoptosisen_US
dc.subjectDoxorubicinen_US
dc.subjectMagnetic albumin nanoparticleen_US
dc.subjectTargeted drug deliveryen_US
dc.titleIn vitro evaluation of doxorubicin-incorporated magnetic albumin nanospheresen_US
dc.typeArticleen_US
dc.authoridTR115002en_US
dc.institutionauthorZeybek, Ayça-
dc.institutionauthorŞanlı Mohamed, Gülşah-
dc.departmentİzmir Institute of Technology. Chemistryen_US
dc.identifier.volume84en_US
dc.identifier.issue1en_US
dc.identifier.startpage108en_US
dc.identifier.endpage115en_US
dc.identifier.wosWOS:000337665900011en_US
dc.identifier.scopus2-s2.0-84902684883en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1111/cbdd.12300-
dc.identifier.pmid24524300en_US
dc.relation.doi10.1111/cbdd.12300en_US
dc.coverage.doi10.1111/cbdd.12300en_US
dc.identifier.wosqualityQ3-
dc.identifier.scopusqualityQ3-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
crisitem.author.dept04.01. Department of Chemistry-
Appears in Collections:Chemistry / Kimya
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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