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    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.csmu.edu.tw:8080/ir/handle/310902500/21008


    题名: Assessing the selective therapeutic efficacy of superparamagnetic erlotinib nanoparticles in lung cancer by using quantitative magnetic resonance imaging and a nuclear factor kappa-B reporter gene system
    作者: Fei-Ting Hsu;Hua-Shan Liu;Ahmed Atef Ahmed Ali;Ping-Huei Tsai;Yu-Chieh Kao;Chia-Feng Lu;Hsu-Shan Huang;Cheng-Yu Chen
    贡献者: 醫學影像暨放射科學系
    关键词: ErlotinibSuperparamagnetic iron oxideMagnetic resonance imagingNuclear factor-κBNon-small-cell lung cancer
    日期: 2017-10-17
    上传时间: 2020-08-06T05:16:18Z (UTC)
    出版者: Nanomedicine: Nanotechnology, Biology and Medicine
    摘要: AbstractNon-small-cell lung cancer (NSCLC) is the most common type of lung cancer. Epidermal growth factor receptor (EGFR) tyrosine kinaseinhibitors are commonly used as the first-line treatment for advanced NSCLC; however, the efficacy of drug delivery remains unknown.Hence, we successfully developed erlotinib-conjugated iron oxide nanoparticles (FeDC-E NPs) as theranostic probe that can potentiallyprovide a new avenue for monitoring drug delivering through noninvasive magnetic resonance imaging. MRIΔR2* relaxivity measurementsoffer an opportunity to quantitatively evaluate the uptake of FeDC-E NPs at cellular and tumoral levels. Additionally, NF-κB reporter genesystem provides NF-κB activation status monitoring to validate the therapeutic efficiency of FeDC-E NPs. FeDC-E NPs not only inhibit thetumor growth and NF-κB-modulated antiapoptotic mechanism but also trigger extrinsic and intrinsic apoptotic pathways. Taken together,dual functional FeDC-E NPs offer diagnostic and therapeutic benefits against lung cancers, indicating that our presented probe could be applied in clinical.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/21008
    關聯: Nanomedicine: Nanotechnology, Biology and Medicine Volume 14, Issue 3, April 2018, Pages 1019-1031
    显示于类别:[醫學影像暨放射科學系暨碩士班] 期刊論文

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