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Complexation with C60 Fullerene Increases Doxorubicin Efficiency against Leukemic Cells In Vitro

机译:与C60富勒烯络合可提高阿霉素体外抗白血病细胞的效率

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摘要

Conventional anticancer chemotherapy is limited because of severe side effects as well as a quickly evolving multidrug resistance of the tumor cells. To address this problem, we have explored a C60 fullerene-based nanosized system as a carrier for anticancer drugs for an optimized drug delivery to leukemic cells.Here, we studied the physicochemical properties and anticancer activity of C60 fullerene noncovalent complexes with the commonly used anticancer drug doxorubicin. C60-Doxorubicin complexes in a ratio 1:1 and 2:1 were characterized with UV/Vis spectrometry, dynamic light scattering, and high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The obtained analytical data indicated that the 140-nm complexes were stable and could be used for biological applications. In leukemic cell lines (CCRF-CEM, Jurkat, THP1 and Molt-16), the nanocomplexes revealed ≤ 3.5 higher cytotoxic potential in comparison with the free drug in a range of nanomolar concentrations. Also, the intracellular drug’s level evidenced C60 fullerene considerable nanocarrier function.The results of this study indicated that C60 fullerene-based delivery nanocomplexes had a potential value for optimization of doxorubicin efficiency against leukemic cells.
机译:由于严重的副作用以及肿瘤细胞快速发展的多药耐药性,常规的抗癌化学疗法受到限制。为了解决这个问题,我们探索了一种基于C60富勒烯的纳米系统作为抗癌药物的载体,以优化向白血病细胞的药物输送。在这里,我们研究了具有常用抗癌作用的C60富勒烯非共价复合物的理化性质和抗癌活性。药物阿霉素。用UV / Vis光谱,动态光散射和高效液相色谱-串联质谱(HPLC-MS / MS)表征1:1和2:1比率的C60-阿霉素复合物。获得的分析数据表明140nm复合物是稳定的并且可以用于生物学应用。在白血病细胞系(CCRF-CEM,Jurkat,THP1和Molt-16)中,在一定的纳摩尔浓度下,与游离药物相比,纳米复合物的细胞毒性潜力≤3.5。同样,细胞内药物的水平证明了C60富勒烯具有相当大的纳米载体功能。这项研究结果表明,基于C60富勒烯的递送纳米复合物对于优化阿霉素对抗白血病细胞的效率具有潜在价值。

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