Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Center for Research of Endemic Parasites of Iran, Tehran University of Medical Sciences, Tehran, Iran.
Mikrochim Acta. 2023 Aug 24;190(9):367. doi: 10.1007/s00604-023-05928-3.
An electrochemical immunosensor based on carbon nanofibers (CNFs) and gold nanoparticles (AuNPs) was developed for detecting anti-Toxoplasma gondii antibodies (anti-T. gondii) IgG in human serum. CNFs were produced using electrospinning and carbonization processes. Screen-printed carbon electrode (SPCE) surface was modified with CNFs and AuNPs which were electrodeposited onto the CNFs. Then, T. gondii antigen was immobilized onto the AuNPs/CNFs/SPCE. Afterward, anti-T. gondii IgG positive serum samples were coated on the modified electrode and assessed via adding anti-human IgG labeled with horseradish peroxidase (HRP) enzyme. The morphology of SPCE, CNFs, and AuNPs/CNFs/SPCE surface was characterized using field emission scanning electron microscopy (FESEM) equipped with energy dispersive spectroscopy (EDS). Characterization of CNFs was evaluated by Raman spectroscopy and X-ray diffraction (XRD). Electrochemical characterization of the immunosensor was verified using cyclic voltammetry (CV), and electrochemical response of modified electrode for anti-T. gondii IgG was detected via differential pulse voltammetry (DPV). This immunosensor was detected in the range 0-200 U mL with a low detection limit (9 × 10 U mL). In addition, the proposed immunosensor was exhibited with high selectivity, strong stability, and acceptable reproducibility and repeatability. Furthermore, there was a strong correlation between results obtained via the designed immunosensor and enzyme-linked immunosorbent assay (ELISA) as gold standard. In conclusion, the developed immunosensor is a promising route for rapid and accurate clinical diagnosis of toxoplasmosis.
基于碳纳米纤维 (CNFs) 和金纳米粒子 (AuNPs) 的电化学免疫传感器被开发用于检测人血清中的抗弓形虫抗体 (anti-T. gondii) IgG。CNFs 通过静电纺丝和碳化工艺制备。通过将 CNFs 和 AuNPs 电沉积到其上,对丝网印刷碳电极 (SPCE) 表面进行修饰。然后,将弓形虫抗原固定在 AuNPs/CNFs/SPCE 上。随后,将抗弓形虫 IgG 阳性血清样品涂覆在修饰电极上,并通过加入辣根过氧化物酶 (HRP) 标记的抗人 IgG 进行评估。使用配备能量色散光谱仪 (EDS) 的场发射扫描电子显微镜 (FESEM) 对 SPCE、CNFs 和 AuNPs/CNFs/SPCE 表面的形态进行了表征。通过拉曼光谱和 X 射线衍射 (XRD) 评估 CNFs 的特性。通过循环伏安法 (CV) 验证了免疫传感器的电化学特性,并通过差分脉冲伏安法 (DPV) 检测了修饰电极对抗弓形虫 IgG 的电化学响应。该免疫传感器在 0-200 U mL 范围内具有较低的检测限 (9 × 10 U mL)。此外,该免疫传感器表现出高选择性、强稳定性和可接受的重现性和重复性。此外,设计的免疫传感器与酶联免疫吸附测定 (ELISA) 作为金标准获得的结果之间存在很强的相关性。总之,所开发的免疫传感器为快速准确的弓形虫临床诊断提供了一种有前途的方法。