School of Food Science and Technology, Henan University of Technology, Lianhua Road 100#, Zhengzhou High & New Technology Industries Development Zone, Zhengzhou, 450001, Henan Province, People's Republic of China.
Mikrochim Acta. 2020 Apr 18;187(5):274. doi: 10.1007/s00604-020-04244-4.
An aptasensor assay for sulfamethazine is introduced based on a gold electrode modified with multi-walled carbon nanotubes@graphene oxide nanoribbons (MWCNTs@GONRs) nanocomposites. The MWCNTs@GONRs nanocomposites were synthesized by a chemical longitudinal partially unzipping method. Its properties are characterized by scanning electron microscope (SEM), energy dispersive spectrometric analysis (EDS), transmission electron microscope (TEM) and X-ray diffraction (XRD). In the presence of sulfamethazine, the conformation of the aptamer changes and a G-quadruplex structure is formed. It inhibits the electron transfer of the redox probe [Fe(CN)] on the electrode surface, causing weakening of the peak current response at the peak potential of 0.17 V (vs. Ag/AgCl). Using differential pulse voltammetry, a linear response was obtained for sulfamethazine concentrations in the range 0.01 ~ 50 ng mL with a detection limit of 5.2 pg mL. Graphical abstract Schematic representation of an electrochemical aptasensor for sulfamethazine determination. A gold electrode is modified with multi-walled carbon nanotubes@graphene oxide nanoribbons to improve the electrode performance. When the aptamer binds to sulfamethazine to form G-quadruplex, the peak current response decreases.
基于金电极修饰的多壁碳纳米管/氧化石墨烯纳米带(MWCNTs@GONRs)纳米复合材料,提出了一种磺胺嘧啶的适体传感器测定法。MWCNTs@GONRs 纳米复合材料通过化学纵向部分解拉链法合成。通过扫描电子显微镜(SEM)、能谱分析(EDS)、透射电子显微镜(TEM)和 X 射线衍射(XRD)对其性质进行了表征。在磺胺嘧啶存在下,适体的构象发生变化,形成 G-四链体结构。它抑制了电极表面上氧化还原探针[Fe(CN)]的电子转移,导致在 0.17 V(相对于 Ag/AgCl)的峰电位处的峰电流响应减弱。使用差分脉冲伏安法,磺胺嘧啶浓度在 0.01 至 50 ng mL 范围内得到线性响应,检测限为 5.2 pg mL。