Tang Dianping, Yuan Ruo, Chai Yaqin
Key Laboratory of Analytical Chemistry (Chongqing), College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, People's Republic of China.
Anal Chem. 2008 Mar 1;80(5):1582-8. doi: 10.1021/ac702217m. Epub 2008 Jan 26.
A new signal amplification strategy based on thionine (TH)-doped magnetic gold nanospheres as labels and horseradish peroxidase (HRP) as enhancer holds promise to improve the sensitivity and detection limit of the immunoassay for carcinoembryonic antigen (CEA), as a model protein. This immunoassay system was fabricated on a carbon fiber microelectrode (CFME) covered with a well-ordered anti-CEA/protein A/nanogold architecture. The reverse micelle method was initially used for the preparation of TH-doped magnetic gold nanospheres (nanospheres), and the synthesized nanospheres were then labeled on HRP-bound anti-CEA as a secondary antibody (bionanospheres). Sandwich-type protocol was successfully introduced to develop a new high-efficiency electrochemical immunoassay with the labeled bionanospheres toward the reduction of H2O2. Under optimized conditions, the linear range of the proposed immunoassay without HRP as enhancer was 1.2-125 ng/mL CEA, whereas the assay sensitivity by using HRP as enhancer could be further increased to 0.01 ng/mL with the linear range from 0.01 to 160 ng/mL CEA. The developed immunoassay method showed good precision, high sensitivity, acceptable stability and reproducibility, and could be used for the detection of real samples with consistent results in comparison with those obtained by the enzyme-linked immunosorbent assay (ELISA) method.
一种基于硫堇(TH)掺杂磁性金纳米球作为标记物、辣根过氧化物酶(HRP)作为增强剂的新型信号放大策略,有望提高作为模型蛋白的癌胚抗原(CEA)免疫分析的灵敏度和检测限。该免疫分析系统构建在覆盖有有序抗CEA/蛋白A/纳米金结构的碳纤维微电极(CFME)上。最初采用反相胶束法制备TH掺杂磁性金纳米球(纳米球),然后将合成的纳米球标记在与HRP结合的抗CEA作为二抗上(生物纳米球)。成功引入夹心型检测方案,以标记的生物纳米球开发了一种新型高效电化学免疫分析方法,用于检测H2O2的还原。在优化条件下,所提出的无HRP作为增强剂的免疫分析线性范围为1.2 - 125 ng/mL CEA,而使用HRP作为增强剂时,检测灵敏度可进一步提高到0.01 ng/mL,线性范围为0.01至160 ng/mL CEA。所开发的免疫分析方法具有良好的精密度、高灵敏度、可接受的稳定性和重现性,并且与酶联免疫吸附测定(ELISA)方法相比,可用于实际样品检测,结果一致。