A signal‐enhanced label‐free electrochemical immunosensor was constructed by the employment of Prussian blue doped silica dioxide (PB‐SiO2) nanocomposite. At first, PB‐SiO2 nanocomposite which was produced by using a microemulsion method was used to obtain a nanostructural monolayer on a glassy carbon electrode (GCE) surface. Next amino‐functionalized interface were prepared by self‐assembling 3‐aminopropyltriethoxy silane (APTES) on the PB‐SiO2 nanoparticle surface. Then chitosan stabled gold nanoparticle (CS‐nanoAu) was subsequently attached, while the entire surface was finally loaded with neuron‐specific enolase antibody (anti‐NSE) via the adsorption of gold nanoparticle. The sensitivity of the proposed immunosensor has greatly improved as the PB‐SiO2 nanostructural sensing film provides plenty of active sites which might catalyze the reduction of H2O2. The immunosensor exhibited good linear behavior in the concentration range from 0.25–5.0 and 5.0–75 ng/mL for the quantitative analysis of neuron‐specific enolase (NSE), a putative serum marker of small‐cell lung carcinoma (SCLC), with a limit of detection of 0.08 ng/mL. The resulting NSE immunosensor showed high sensitivity and long‐term lifetime which can be attributed to the extremely high catalytic activity and biocompatibility of CS‐nanoAu/APTES/PB‐SiO2 nanostructural multilayers. 相似文献
In this paper, a novel amperometric immunosensor for the determination of carbofuran based on gold nanoparticles (GNPs), magnetic Fe3O4 nanoparticles-functionalized multiwalled carbon nanotubes-chitosan (Fe3O4-FCNTs-CS), and bovine serum albumin (BSA) composite film was proposed. First, GNPs were immobilized onto the glassy carbon electrode (GCE) surface, and then the magnetic Fe3O4 nanoparticles mixed with chitosan-functionalized multiwall carbon nanotubes (CS-FCNTs) homogeneous composite (CS-FCNTs-Fe3O4) was immobilized onto the GNPs layer by electrostatic interactions between amino groups of CS and GNPs. Because chitosan (CS) contains many amino groups, it can absorb more antibodies. FCNTs have high surface area, high electrical conductivity, and it can enhance the electron transfer rate; Magnetite (Fe3O4) nanoparticles can provide a favorable microenvironment for biomolecules immobilization due to their good biocompatibility, strong superparamagnetic property, and low toxicity; and GNPs possess high surface-to-volume reaction, stability, and high conductivity. Gold Nanoparticles/Fe3O4-FCNTs-CS composite film was constructed onto the GCE surface, which had significant synergistic effects toward immunoreaction signal amplification. The stepwise assembly process was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), respectively. Under the optimal conditions, the current response was proportional to the concentration of carbofuran ranging from 1.0 ng/mL to 100.0 ng/mL and from 100.0 ng/mL to 200 µg/mL with the detection limit 0.032 ng/mL. The proposed immunosensor exhibited good accuracy, high sensitivity, and stability, and it can be used for detection of carbofuran pesticide. 相似文献
A novel type of Fe3O4 nanoparticles modified glass carbon electrode(Fe3O4/GCE) was constructed and the electrochemical properties of N-(4-nitro-2-phenoxyphenyl)methanesulfonamide(nimesulide) were studied on the Fe3O4/GCE.In 0.4mol/L HAc-NaAc buffer solution(pH=5.0),the electrode process of nimesulide was irreversible at bare GCE and Fe3O4/GCE.The Fe3O4/GCE exhibited a remarkable catalytic and enhancement effect on the reduction of nimesulide.The reduction peak potential of nimesulide shifted positively from... 相似文献
A novel amperometric immunosensor was developed by immobilizing ferritin antibody (FeAb) on the surface of Fe3O4 magnetic nanoparticles/chitosan composite film modified glassy carbon electrode (GCE). This material combined the advantages
of inorganic Fe3O4 nanoparticles with the organic polymer chitosan. The stepwise assembly procedure of the immunosensor was characterized by
means of differential pulse voltammetry (DPV) and ac impedance. The K3Fe(CN)6/K4Fe(CN)6 was used as a marker to probe the interface and to determinate ferritin. The factors that could influence the performance
of the resulting immunosensor were studied in detail. After the immunosensor was incubated with ferritin for 32 min at 35 °C,
the DPV current decreased linearly with the logarithm of ferritin concentration in the range from 20 to 500 ng mL−1 with a correlation coefficient of 0.995 and a detection limit of 7.0 ng mL−1. This immunosensor was used to analyze ferritin in human serum samples. The analytical results showed that the developed
immunoassay was comparable with the radioimmunoassay (RIA), and the studied immunosensor exhibited good accuracy, high sensitivity,
and long-term stability for 3 weeks, which implies a promising alternative approach for detecting ferritin in clinical diagnosis. 相似文献
We are presenting an electrochemical immunosensor for the determination of the β-agonist and food additive ractopamine. A glassy carbon electrode (GCE) was modified with gold nanoparticles and a film of a composite made from poly(arginine) and multi-walled carbon nanotubes. Antibody against ractopamine was immobilized on the surface of the modified GCE which then was blocked with bovine serum albumin. The assembly of the immunosensor was followed by electrochemical impedance spectroscopy. Results demonstrated that the semicircle diameter increases, indicating that the film formed on the surface hinders electron transfer due to formation of the antibody-antigen complex on the modified electrode. Under optimal conditions, the peak current obtained by differential pulse voltammetry decreases linearly with increasing ractopamine concentrations in the 0.1 nmol•L−1 to 1 μmol•L−1 concentration range. The lower detection limit is 0.1 nmol•L−1. The sensor displays good stability and reproducibility. The method was applied to the analysis of spiked swine feed samples and gave satisfactory results.
Immunoassay for ractopamine based on glassy carbon electrode modified with gold nanoparticles and a film of a composite made from poly (arginine) and multi-walled carbon nanotubes was proposed. Under optimal conditions, the peak currents obtained by differential pulse voltammetry decreases linearly with increasing ractopamine concentrations in the 0.1 nmol•L−1 to 1 μmol•L−1 concentration range. The detection limit is 0.1 nmol•L−1.