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Lab-on-a-chip for anticancer drug screening using quantum dots probe based apoptosis assay

机译:使用基于量子点探针的细胞凋亡检测方法进行芯片实验室抗癌药物筛选

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Quantitative data acquisition of the drug induced cell apoptosis is one of the most important aspects of anticancer drug assessment. Traditional methods using photo-bleachable organic dyes to detect the apoptotic cells, may lead to some difficulties in long time observation of the cells. Moreover, the culture plates inevitably require large number of cells resulting in inefficiency in analysis of fewer cell samples such as a patient's own cells. To address these problems, we developed a microfluidic platform to assess the adherent cell cytotoxicity for anticancer drug screening using Annexin V conjugated quantum dots and Calcein AM as dual apoptotic probes. The results showed that camptothecin possessed more potent cytotoxic effect on these adherent tumor cells. Interestingly, the MCF-7 exhibited a certain resistance to these two anti-tumor drugs. For the first time, we achieved the evaluation of the impacts of model anti-cancer drugs on different adherent tumor cell lines using bio-functional quantum dots probe based cytotoxicity assays in a microfluidic device.
机译:药物诱导的细胞凋亡的定量数据采集是抗癌药物评估最重要的方面之一。使用光致漂白有机染料检测凋亡细胞的传统方法可能会导致长时间观察细胞方面的困难。此外,培养板不可避免地需要大量细胞,导致分析较少的细胞样品(例如患者自身细胞)的效率低下。为了解决这些问题,我们开发了一种微流控平台,以使用Annexin V共轭量子点和Calcein AM作为双重凋亡探针评估粘附细胞的细胞毒性,以进行抗癌药物筛选。结果表明喜树碱对这些粘附的肿瘤细胞具有更强的细胞毒性作用。有趣的是,MCF-7对这两种抗肿瘤药物表现出一定的抵抗力。我们首次在微流控设备中使用基于生物功能量子点探针的细胞毒性测定法评估了模型抗癌药对不同粘附肿瘤细胞系的影响。

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