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Optical nanotechnology enables rapid label-free diagnostics for cancer biomarker screening

机译:光学纳米技术可以为癌症生物标志物筛查提供快速的无标记诊断

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A high-accuracy biosensor system has been developed to provide rapid detection of biomarker proteins as indicators of ovarian cancer. This photonic detection system is based upon guided-mode resonance sensor technology. The buildup of the attaching biolayer can be monitored directly, without use of chemical tags, by following the corresponding resonance shift with a spectrometer or detector array. Additionally, these high-resolution sensors employ multiple resonance peaks at identical physical location on the sensor surface. Each of these resonance peaks responds uniquely to the detection event, thereby enriching the data set available for quantification. The peaks result from individual, polarization-dependent resonant leaky modes that are the foundation of this technology. Examples are presented for detection of ovarian cancer biomarkers (fibronectin and apoliprotein A-1) in serum and cell culture supernatant, with detection sensitivities to ~20 ng/ml. Minimal nonspecific binding was measured in cell media and serum backgrounds. We also present an example dual-polarization resonance response with corresponding backfitting results that illustrate the capability to distinguish between changes at the sensor surface due to biolayer adhesion and those due to sample background changes.
机译:已经开发出一种高精度的生物传感器系统,以提供快速检测生物标志物蛋白作为卵巢癌的指标。该光子检测系统基于引导模式谐振传感器技术。通过使用光谱仪或探测器阵列的相应的共振偏移,可以直接监测附接Biolayer的构建,而不使用化学标签。另外,这些高分辨率传感器在传感器表面上的相同物理位置采用多个谐振峰。这些共振峰中的每一个唯一地响应检测事件,从而富集可用于量化的数据集。峰值由依赖于该技术的基础的个体,极化依赖性谐振泄漏模式。提出了在血清和细胞培养上清液中检测卵巢癌生物标志物(纤维连接蛋白和脂肪蛋白A-1)的实例,检测敏感性至约20ng / ml。在细胞培养基和血清背景下测量最小的非特异性结合。我们还提出了一种示例性双极化共振响应,其具有相应的回合结果,其示出了由于Biolayer粘附而在传感器表面的变化和由于样品背景变化而区分传感器表面的变化的能力。

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