Chongqing Key Laboratory of Analytical Chemistry, College of Chemistry, Chongqing, People's Republic of China.
Bioprocess Biosyst Eng. 2010 Feb;33(2):179-85. doi: 10.1007/s00449-009-0302-4. Epub 2009 Feb 17.
AuCl(4) was initially deposited by electrochemical reduction on a glassy carbon electrode (GCE) to form porous nanogold layer, then prussian blue (PB) was electrodeposited onto the as-prepared nanogold layer, and then secondary nanogold particles were fabricated again on the PB surface by electrochemical reduction for the immobilization of anti-CEA antibodies. The presence of double-layer porous gold nanoparticles enhanced the immobilized amount of biomolecules, and improved the sensitivity of the immunoassay. PB, as a good redox probe, was facile to electrochemical analysis and measurement. Under optimal conditions, the developed immunoassay exhibited dynamic range from 3.0 to 80.0 ng/mL with a detection limit of 0.9 ng/mL CEA (S/N = 3). Moreover, the selectivity, reproducibility and stability of the immunosensor were acceptable.
AuCl(4) 最初通过电化学还原沉积在玻碳电极 (GCE) 上,形成多孔纳米金层,然后将普鲁士蓝 (PB) 电沉积到所制备的纳米金层上,然后通过电化学还原再次在 PB 表面制备二次纳米金颗粒,用于固定抗 CEA 抗体。双层多孔金纳米粒子的存在增加了生物分子的固定量,并提高了免疫分析的灵敏度。PB 作为一种良好的氧化还原探针,易于电化学分析和测量。在最佳条件下,所开发的免疫分析从 3.0 到 80.0ng/mL 具有动态范围,检测限为 0.9ng/mL CEA(S/N = 3)。此外,该免疫传感器的选择性、重现性和稳定性是可以接受的。