Biomicrofluidics. 2011 Feb 15;5(1):14102. doi: 10.1063/1.3553014.
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.
通过微流控技术实现免疫分析的小型化有可能减少分析所需的时间和反应物的量,同时有可能实现多重检测和便携性。本研究将薄膜非晶硅(a-Si:H)光电二极管与薄膜非晶硅-碳合金集成在玻璃衬底上,薄膜非晶硅-碳合金直接沉积在光电二极管上方,作为荧光滤光片,制作成的芯片与基于聚二甲基硅氧烷的微流控网络集成,用于直接检测使用荧光标记的抗体-抗原分子识别反应。使用的模型免疫分析包括将一抗吸附到微通道壁上,然后由与荧光量子点标签标记的二抗识别。定义了微流控格式中的流动分析条件,总分析时间为 30 分钟。定量检测到了特异性分子识别。a-Si:H 光电二极管的测量结果与荧光显微镜的测量结果一致,均显示出在纳摩尔-微摩尔范围内与抗体浓度的线性关系。