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Heterogeneous immunoassays in microfluidic format using fluorescence detection with integrated amorphous silicon photodiodes

机译:使用集成非晶硅光电二极管的荧光检测以微流体形式进行异质免疫测定

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摘要

Miniaturization of immunoassays through microfluidic technology has the potential to decrease the time and the quantity of reactants required for analysis, together with the potential of achieving multiplexing and portability. A lab-on-chip system incorporating a thin-film amorphous silicon (a-Si:H) photodiode microfabricated on a glass substrate with a thin-film amorphous silicon-carbon alloy directly deposited above the photodiode and acting as a fluorescence filter is integrated with a polydimethylsiloxane-based microfluidic network for the direct detection of antibody-antigen molecular recognition reactions using fluorescence. The model immunoassay used consists of primary antibody adsorption to the microchannel walls followed by its recognition by a secondary antibody labeled with a fluorescent quantum-dot tag. The conditions for the flow-through analysis in the microfluidic format were defined and the total assay time was 30 min. Specific molecular recognition was quantitatively detected. The measurements made with the a-Si:H photodiode are consistent with that obtained with a fluorescence microscope and both show a linear dependence on the antibody concentration in the nanomolar-micromolar range.
机译:通过微流体技术使免疫测定法小型化,有可能减少分析所需的时间和反应物的数量,并具有实现多重性和便携性的潜力。集成了一个芯片实验室系统,该系统集成了在玻璃基板上微细加工的薄膜非晶硅(a-Si:H)光电二极管和直接沉积在光电二极管上方并用作荧光滤光片的薄膜非晶硅-碳合金基于聚二甲基硅氧烷的微流体网络,可使用荧光直接检测抗体-抗原分子识别反应。所用的模型免疫测定法包括:一抗吸附到微通道壁上,然后被标记有荧光量子点标签的二抗识别。定义了以微流体形式进行流通分析的条件,总分析时间为30分钟。定量检测特异性分子识别。用a-Si:H光电二极管进行的测量与通过荧光显微镜获得的测量结果一致,并且都显示出在纳摩尔-微摩尔范围内对抗体浓度的线性依赖性。

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