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首页> 外文期刊>IEEE Transactions on Biomedical Engineering >Nanoscale Quantifying the Effects of Targeted Drug on Chemotherapy in Lymphoma Treatment Using Atomic Force Microscopy
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Nanoscale Quantifying the Effects of Targeted Drug on Chemotherapy in Lymphoma Treatment Using Atomic Force Microscopy

机译:使用原子力显微镜对淋巴瘤治疗中靶向药物对化学疗法的纳米量化。

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摘要

The applications of targeted drugs in treating cancers have significantly improved the survival rates of patients. However, in the clinical practice, targeted drugs are commonly combined with chemotherapy drugs, causing that the exact contribution of targeted drugs to the clinical outcome is difficult to evaluate. Quantitatively investigating the effects of targeted drugs on chemotherapy drugs on cancer cells is useful for us to understand drug actions and design better drugs. The advent of atomic force microscopy (AFM) provides a powerful tool for probing the nanoscale physiological activities of single live cells. In this paper, the detailed changes in cell morphology and mechanical properties were quantified on single lymphoma cells during the actions of rituximab (a monoclonal antibody targeted drug) and two chemotherapy drugs (cisplatin and cytarabine) by AFM. AFM imaging revealed the distinct changes of cellular ultramicrostructures induced by the drugs. The changes of cellular mechanical properties after the drug stimulations were measured by AFM indenting. The statistical histograms of cellular surface roughness and mechanical properties quantitatively showed that rituximab could remarkably strengthen the killing effects of chemotherapy drugs. The study offers a new way to quantify the synergistic interactions between targeted drugs and chemotherapy drugs at the nanoscale, which will have potential impacts on predicting the efficacies of drug combinations before clinical treatments.
机译:靶向药物在治疗癌症中的应用显着提高了患者的存活率。然而,在临床实践中,靶向药物通常与化疗药物联合使用,导致难以评估靶向药物对临床结果的确切贡献。定量研究靶向药物对癌细胞化疗药物的作用对于我们了解药物作用和设计更好的药物很有用。原子力显微镜(AFM)的出现为探测单个活细胞的纳米级生理活性提供了强大的工具。在本文中,通过AFM对利妥昔单抗(一种单克隆抗体靶向药物)和两种化疗药物(顺铂和阿糖胞苷)作用期间单个淋巴瘤细胞的细胞形态和力学特性的详细变化进行了定量。原子力显微镜成像揭示了药物诱导的细胞超微结构的明显变化。通过AFM压痕测量药物刺激后的细胞力学性能变化。细胞表面粗糙度和机械性能的统计直方图定量显示,利妥昔单抗可以显着增强化疗药物的杀伤作用。这项研究提供了一种新方法,可以量化纳米级靶向药物与化学疗法药物之间的协同相互作用,这将对预测临床治疗之前药物组合的疗效产生潜在影响。

著录项

  • 来源
    《IEEE Transactions on Biomedical Engineering》 |2016年第10期|2187-2199|共13页
  • 作者单位

    State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences;

    Department of Lymphoma, Affiliated Hospital of Military Medical Academy of Sciences;

    State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences, Shenyang, China;

    State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences;

    State Key Laboratory of Robotics, Shenyang Institute of Automation, Chinese Academy of Sciences;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Drugs; Force; Microscopy; Chemotherapy; Nanoscale devices; Young's modulus;

    机译:药物;力;显微镜;化学疗法;纳米级器械;杨氏模量;

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