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Nuclear mapping of nanodrug delivery systems in dynamic cellular environments

机译:动态细胞环境中纳米药物递送系统的核图

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Nanoformulations have shown great promise for delivering chemotherapeutics and hold tremendous clinical relevance. However nuclear mapping of the chemodrugs is important to predict the success of the nanoformulation. In this study fluorescence microscopy and a subcellular tracking algorithm were used to map the diffusion of chemotherapeutic drugs in cancer cells. Positively charged nanoparticles efficiently carried the chemodrug across the cell membrane. The algorithm helped map free drug and drug-loaded nanoparticles, revealing a varying nuclear diffusion pattern of the chemotherapeutics in drug-sensitive and -resistant cells in a live dynamic cellular environment. While the drug-sensitive cells showed an exponential uptake of the drug with time, resistant cells showed random and asymmetric drug distribution. Moreover nanoparticles carrying the drug remained in the perinuclear region, while the drug accumulated in the cell nuclei. The tracking approach has enabled us to predict the therapeutic success of different nanoscale formulations of doxorubicin.
机译:纳米制剂已显示出提供化学治疗的巨大前景,并具有巨大的临床意义。然而,化学药品的核图对于预测纳米制剂的成功很重要。在这项研究中,使用荧光显微镜和亚细胞跟踪算法来绘制化疗药物在癌细胞中的扩散图。带正电荷的纳米粒子有效地将化学药物跨细胞膜运送。该算法帮助绘制了游离药物和载有药物的纳米颗粒的图谱,揭示了在动态动态细胞环境中对药物敏感和耐药的细胞中化学治疗药物的不同核扩散模式。虽然药物敏感性细胞显示药物随时间呈指数吸收,但耐药细胞显示药物分布随机且不对称。此外,携带药物的纳米颗粒保留在核周区域,而药物则积累在细胞核中。跟踪方法使我们能够预测阿霉素的不同纳米级制剂的治疗成功。

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