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ASSESSMENT OF CANCER TARGETING POTENTIAL OF DOXORUBICIN CONJUGATED WITH SURFACE FUNCTIONALIZED MULTI-WALLED CARBON NANOTUBES

机译:与表面官能化多壁碳纳米管缀合的多柔比星的癌症靶向电位评估

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摘要

Our main aim in the present investigation was to assess the cancer targeting potential of doxorubicin conjugated with folic acid (FA), ethylene di-amine (EDA) and surface F- MWCNTs (FA-EDA-MWCNTs-DOX) conjugate employing on MCF-7 (breast cancer cell line) for efficient tumor targeting. We developed a highly effective novel targeted drug delivery based on DOX-conjugated with the surface of F-MWCNTs by using nucleophilic substitution reaction mechanism and evaluated in facile strategy for cancer treatment. The in vitro drug release study shows that the percentage of drug release under an acidic condition pH-5.4 is higher than that under normal physiological conditions. The FA-EDA-MWCNTs-DOX nano-conjugate affords higher efficacy in tumor growth suppression due to its stealth nature and most preferentially taken up by cultured MCF-7 cells through receptor-mediated endocytosis mechanism. Fourier Transform Infrared Spectroscopy (FTIR), UV-Visible Spectroscopy, Nuclear Magnetic Resonance Spectroscopy (NMR) and Scanning Electron Microscopy (SEM) measurements clearly confirmed the functionalization & conjugation steps. The results concluded that developed water-soluble nano-conjugate might emerge as "safe and effective" nano-medicine in cancer treatment by minimizing the side effects with generally regarded as a safe prominence.
机译:我们在本研究的主要目的是评估与叶酸(Fa),乙烯二胺(EDA)和表面F-MWCNT(FA-EDA-MWCNTS-DOX)缀合物缀合的多柔比星的癌症靶向电位(FA-EDA-MWCNTS-DOX)缀合物在MCF上7(乳腺癌细胞系)用于高效肿瘤靶向。我们通过使用亲核取代反应机制,基于与F-MWCNT的表面的Dox-缀合的高效新型针对性药物递送,并在癌症治疗中进行了评估。体外药物释放研究表明,酸性条件pH-5.4下的药物释放百分比高于正常生理条件下的百分比。由于其隐身性质,Fa-EDA-MWCNTS-DOX纳米缀合物在肿瘤生长抑制中具有更高的疗效,并且通过受体介导的内吞作用机制,培养的MCF-7细胞最优先占用。傅里叶变换红外光谱(FTIR),UV可见光谱,核磁共振光谱(NMR)和扫描电子显微镜(SEM)测量清楚地证实了官能化和共轭步骤。结论的结果,通过最小化通常被认为是安全突出的副作用,可以出现出现水溶性纳米缀合物的水溶性纳米缀合物的纳米医学。

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