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dc.contributor.authorDanısman-Kalındemirtas¸Ferdane
dc.contributor.authorKariper, I.Afsin
dc.contributor.authorHepokur, Ceylan
dc.contributor.authorErdem-Kuruca,Serap
dc.date.accessioned2022-05-18T12:19:19Z
dc.date.available2022-05-18T12:19:19Z
dc.date.issued2021tr
dc.identifier.citationFerdane Danıs¸man-Kalındemirtas¸ a, ˙I.Afs¸in Kari˙per b,*, Ceylan Hepokur c, Serap Erdem-Kuruca a a Istanbul University, Istanbul Faculty of Medicine, Department of Physiology, Istanbul, Turkey b Erciyes University, Education Faculty, Department of Sience Education, Kayseri, Turkey c Cumhuriyet University, Pharmacy Faculty, Department of Biochemistry, Sivas, Turkeytr
dc.identifier.urihttps://hdl.handle.net/20.500.12418/13212
dc.description.abstractPaclitaxel (PTX) is one of the most effective drugs in the treatment of cancer. However, its usability is limited due to low solubility and side effects. In this study, we investigated anticancer effects of PTX bonded silver nano particles (AgNPs-PTX) on 4 different cancer cells, namely MDA-MB-231, MCF-7, 4T1, Saos-2, and on non cancerous HUVEC cells. The silver nanoparticles (AgNPs) that we synthesized were first characterized by UV VIS, FTIR, SEM, and DLS analysis. The size of AgNPs was measured to be around 3 nm and AgNPs-PTX around 10 nm. AgNPs-PTX were found to be 2 to 10 times more effective than PTX alone. Especially, Saos-2 cells were found to be approximately 10 times more sensitive to AgNPs-PTX than PTX alone. AgNPs-PTX did not caused toxicity on non-cancerous HUVEC cell and significantly reduced the viability of all cancer cells we tested. Our findings suggest that AgNPs-PTX may be an anticancer agent candidate that is more effective than PTX alone and specific to Saos-2 cells.tr
dc.rightsinfo:eu-repo/semantics/closedAccesstr
dc.subjectSilver nanoparticles Cytotoxicity Paclitaxel Cancer cell lines Saos-2tr
dc.titleSelective cytotoxicity of paclitaxel bonded silver nanoparticle on different cancer cellstr
dc.typearticletr
dc.contributor.departmentEczacılık Fakültesitr
dc.relation.publicationcategoryRaportr


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