School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian, 116029, China.
School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian, 116029, China.
Talanta. 2021 May 1;226:122160. doi: 10.1016/j.talanta.2021.122160. Epub 2021 Jan 29.
Immunoglobulin G (IgG) is related to the occurrence of many diseases, such as measles and inflammatory. In this paper, IgG imprinted polymers (IgGIPs) were fabricated on the surface of nano Au/nano Ni modified Au electrode (IgGIPs/AuNCs/NiNCs/Au) via metal-free visible-light-induced atom transfer radical polymerization (MVL ATRP). The IgGIPs were prepared by IgG conjugated with fluorescein isothiocyanate (FITC-IgG) as both a template and a photocatalyst. After the templates were removed, the photocatalysts (FITC) would not remain in the polymer and avoided all the effect of catalysts on the electrode. The fabricated electrodes were examined by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). Under the optimized conditions, IgGIPs/AuNCs/NiNCs/Au was prepared and used as an electrochemical biosensor. The biosensor could be successfully applied for the determination of IgG by differential pulse voltammetry (DPV) measurement. The results showed that the proposed biosensor displayed a broader linear range and a lower detection limit for IgG determination when it was compared to those similar IgG sensors. The linear range from 1.0 × 10 mg L to 1.0 × 10 mg L was obtained with a low detection limit (LOD) of 2.0 × 10 mg L (S/N = 3). Briefly, the biosensor in this study introduced an easy and non-toxic method for IgG determination and also provided a progressive approach for designing protein imprinted polymers.
免疫球蛋白 G(IgG)与许多疾病的发生有关,例如麻疹和炎症。在本文中,通过无金属可见光诱导原子转移自由基聚合(MVL ATRP),在纳米 Au/纳米 Ni 修饰的 Au 电极表面制备了 IgG 印迹聚合物(IgGIPs)。IgGIPs 是通过将荧光素异硫氰酸酯(FITC-IgG)与 IgG 偶联作为模板和光催化剂来制备的。模板去除后,光催化剂(FITC)将不会留在聚合物中,从而避免了催化剂对电极的所有影响。通过循环伏安法(CV)、电化学阻抗谱(EIS)、扫描电子显微镜(SEM)和 X 射线光电子能谱(XPS)对制备的电极进行了检查。在优化条件下,制备了 IgGIPs/AuNCs/NiNCs/Au,并将其用作电化学生物传感器。通过差分脉冲伏安法(DPV)测量成功地将该生物传感器应用于 IgG 的测定。结果表明,与类似的 IgG 传感器相比,该生物传感器在用于 IgG 测定时具有更宽的线性范围和更低的检测限。从 1.0×10mgL 到 1.0×10mgL 获得了线性范围,检测限(LOD)低至 2.0×10mgL(S/N=3)。总之,本研究中的生物传感器为 IgG 的测定引入了一种简单且无毒的方法,也为设计蛋白质印迹聚合物提供了一种渐进的方法。