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dc.contributor.authorIslamian, JP
dc.contributor.authorHatamian, M
dc.contributor.authorAval, NA
dc.contributor.authorRashidi, MR
dc.contributor.authorMesbahi, A
dc.contributor.authorMohammadzadeh, M
dc.contributor.authorJafarabadi, MA
dc.date.accessioned2018-08-26T07:19:30Z
dc.date.available2018-08-26T07:19:30Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/45623
dc.description.abstractIntroduction: Nanoparticles are promising as a new approach to enhance chemo-radiotherapy efficiency in breast cancer mainly via targeted therapy. Materials & methods: SKBR3 and T47D breast cancer cells were treated with superparamagnetic mew porous hydroxyapatite nanocomposites (SPmHANs)conjugated with 1 mu M doxorubicin and 0.5 mM 2-Deoxy-o-Glucose and irradiated with 1 and 2 Gy gamma rays in vitro. The treatment toxicity and also the apoptosis/necrosis ratio were measured by MIT assay and also ELISA cell death detection PLUS, respectively. Results: The decreased cell viability with the combined treatment, with determined 42% loading efficiency for 200 ppm 2DG and 93% for5ppm doxorubicin on SPmHANs in PH about 7.4 and 5.5, were calculated to 60.9% and 68% compared to radiotherapy alone inT47D and SKBR3 cells (both with p < 0.05), respectively. Conclusion: Breast cancer cure may boost from The combined targeted nanoparticle treatment with doxorubicin and 2-Deoxy-o-Glucose may boost breast cancer radiotherapy by improved chemodrug localization, increased cytotoxicity in tumor cells and decreased single modality treatment doses. (C) 2017 Elsevier Ltd. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofBREAST
dc.subject2-Deoxy-o-Glucose
dc.subjectBreast cancer
dc.subjectChemotherapy
dc.subjectDoxorubicin
dc.subjectNanocomposite
dc.subjectIonizing radiation
dc.titleTargeted superparamagnetic nanoparticles coated with 2-deoxy-D-gloucose and doxorubicin more sensitize breast cancer cells to ionizing radiation
dc.typeArticle
dc.citation.volume33
dc.citation.spage97
dc.citation.epage103
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.breast.2017.03.009


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