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Ultrasensitive clinical enumeration of rare cells ex vivo using a μ-Hall detector

机译:使用μ-霍尔探测器稀有细胞先体外后体内的超灵敏临床枚举

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摘要

The ability to detect rare cells (< 100 cells per ml of whole blood) and obtain quantitative measurements of specific biomarkers on single cells is increasingly important in basic biomedical research. Implementing such methodology for widespread use in the clinic, however, has been hampered by low cell density, small sample sizes, and requisite sample purification. To overcome these challenges, we have developed a microfluidic chip-based micro-Hall detector (μHD), which can directly measure single, immunomagnetically tagged cells in whole blood. The μHD can detect single cells even in the presence of vast numbers of blood cells and unbound reactants, and does not require any washing or purification steps. In addition, the high bandwidth and sensitivity of the semiconductor technology used in the μHD enables high-throughput screening (currently ~107 cells/min). The clinical utility of the μHD chip was demonstrated by detecting circulating tumor cells in whole blood of 20 ovarian cancer patients at higher sensitivity than currently possible with clinical standards. Furthermore, the use of a panel of magnetic nanoparticles, distinguished with unique magnetization properties and bio-orthogonal chemistry, allowed simultaneous detection of the biomarkers EpCAM, HER2eu, and EGFR on individual cells. This cost-effective, single-cell analytical technique is well-suited to perform molecular and cellular diagnosis of rare cells in the clinic.
机译:在基础生物医学研究中,检测稀有细胞(每毫升全血<100个细胞)并获得特定生物标志物定量测量的能力在基础生物医学研究中变得越来越重要。但是,由于细胞密度低,样本量小和必需的样本纯化,阻碍了这种方法在临床上的广泛应用。为了克服这些挑战,我们开发了一种基于微流体芯片的微型霍尔检测器(μHD),该检测器可以直接测量全血中单个免疫标记的细胞。 μHD即使在存在大量血细胞和未结合的反应物的情况下也可以检测单个细胞,并且不需要任何清洗或纯化步骤。此外,μHD中使用的半导体技术的高带宽和高灵敏度可实现高通量筛选(目前约为10 7 个细胞/分钟)。 μHD芯片的临床实用性通过检测20例卵巢癌患者全血中的循环肿瘤细胞以高于目前临床标准的灵敏度来证明。此外,使用一组具有独特磁化特性和生物正交化学的磁性纳米粒子,可以同时检测单个细胞上的生物标记EpCAM,HER2 / neu和EGFR。这种具有成本效益的单细胞分析技术非常适合在临床中对稀有细胞进行分子和细胞诊断。

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