Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan 030032, China.
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Molecules. 2023 Nov 19;28(22):7664. doi: 10.3390/molecules28227664.
The rapid and sensitive detection of the important biomarker C-reactive protein (CRP) is of great significance for monitoring inflammation and tissue damage. In this work, an electrochemiluminescence (ECL) aptasensor was fabricated based on dual signal amplification for the sensitive detection of CRP in serum samples. The sensor was constructed by modifying a silica nanochannel array film (SNF) on a cost-effective indium tin oxide (ITO) electrode using the Stöber solution growth method. Gold nanoparticles (AuNPs) were grown in situ within the nanochannels using a simple electrodeposition method as a nanocatalyst to enhance the active electrode area as well as the ECL signal. The negatively charged nanochannels also significantly enriched the positively charged ECL emitters, further amplifying the signal. The recognition aptamer was covalently immobilized on the outer surface of SNF after modification with epoxy groups, constructing the aptasensor. In the presence of CRP, the formation of complexes on the recognitive interface led to a decrease in the diffusion of ECL emitters and co-reactants to the supporting electrode, resulting in a reduction in the ECL signal. Based on this mechanism, ECL detection of CRP was achieved with a linear range of 10 pg/mL to 1 μg/mL and a low limit of detection (7.4 pg/mL). The ECL aptasensor developed in this study offers advantages such as simple fabrication and high sensitivity, making promising applications in biomarker detection.
快速、灵敏地检测重要的生物标志物 C 反应蛋白(CRP)对于监测炎症和组织损伤具有重要意义。在这项工作中,我们制备了一种基于双重信号放大的电化学发光(ECL)适体传感器,用于灵敏检测血清样本中的 CRP。该传感器通过使用 Stöber 溶液生长法在经济实惠的铟锡氧化物(ITO)电极上修饰硅纳米通道阵列膜(SNF)来构建。通过简单的电沉积方法原位生长金纳米粒子(AuNPs)作为纳米催化剂,以增强活性电极面积和 ECL 信号。带负电荷的纳米通道还显著富集了带正电荷的 ECL 发射器,进一步放大了信号。修饰后的 SNF 用环氧基团进行修饰后,将识别适体共价固定在其外表面,构建适体传感器。在 CRP 存在的情况下,识别界面上复合物的形成导致 ECL 发射器和共反应物向支撑电极的扩散减少,从而导致 ECL 信号降低。基于这种机制,实现了 CRP 的 ECL 检测,线性范围为 10 pg/mL 至 1 μg/mL,检测限低至 7.4 pg/mL。本研究开发的 ECL 适体传感器具有制造简单、灵敏度高的优点,在生物标志物检测方面具有广阔的应用前景。