School of Pharmacy, Jiangsu University, Zhenjiang, 212013, People's Republic of China.
The People's Hospital of Danyang, Affiliated Danyang Hospital of Nantong University, Zhenjiang, 212300, People's Republic of China.
Mikrochim Acta. 2023 Dec 29;191(1):64. doi: 10.1007/s00604-023-06117-y.
A "turn-on" aptasensor for label-free and cell-free EpCAM detection was constructed by employing magnetic α-FeO/FeO@Au nanocomposites as a matrix for signal amplification and double-stranded complex (SH-DNA/Apt probes) immobilization through Au-S binding. α-FeO/FeO@Au could be efficiently assembled into uniform and stable self-assembly films via magnetic-induced self-assembly technique on a magnetic glassy carbon electrode (MGCE). The effectiveness of the platform for EpCAM detection was confirmed through differential pulse voltammetry (DPV). Under optimized conditions, the platform exhibited excellent specificity for EpCAM, and a strong linear correlation was observed between the current and the logarithm of EpCAM protein concentration in the range 1 pg/mL-1000 pg/mL (R = 0.9964), with a limit of detection (LOD) of 0.27 pg/mL. Furthermore, the developed platform demonstrated good stability during a 14-day storage test, with fluctuations remaining below 93.33% of the initial current value. Promising results were obtained when detecting EpCAM in spiked serum samples, suggesting its potential as a point-of-care (POC) testing.
构建了一种“开启”适体传感器,用于无标记和无细胞 EpCAM 检测,该传感器通过将磁性 α-FeO/FeO@Au 纳米复合材料作为信号放大和双链复合物 (SH-DNA/Apt 探针) 通过 Au-S 键固定的基质。α-FeO/FeO@Au 可以通过磁性诱导自组装技术在磁性玻碳电极 (MGCE) 上高效组装成均匀且稳定的自组装膜。通过差分脉冲伏安法 (DPV) 验证了该平台用于 EpCAM 检测的有效性。在优化条件下,该平台对 EpCAM 表现出优异的特异性,并且在 1 pg/mL-1000 pg/mL 的范围内,电流与 EpCAM 蛋白浓度的对数之间表现出强烈的线性相关性 (R = 0.9964),检测限 (LOD) 为 0.27 pg/mL。此外,该开发的平台在 14 天储存测试期间表现出良好的稳定性,电流波动保持在初始电流值的 93.33%以下。在检测加标血清样本中的 EpCAM 时获得了有希望的结果,表明其在即时检测 (POC) 中的潜在应用。