A dual amplification electrochemical immunosensor based on HRP-Au@Ag NPs for carcinoembryonic antigen detection.

A sensitive sandwich-type electrochemical immunosensor based on dual amplification strategy was constructed. The dual amplification strategy has been used secondary antibody(Ab2)-horseradish peroxidase(HRP)-Au@Ag nanoparticles (Au@Ag NPs) for carcinoembryonic antigen(CEA) detection. Ab2-HRP-Au@Ag NPs as dual amplification markers triggered the disproportionation of H2O2, which could facilitate the catalytic oxidation of hydroquinone to quinone(BQ). In addition, due to their large surface area and excellent conductivity, nitrogen-doped graphene were used as a platform to firmly assemble primary antibody (Ab1). Above mentioned generated amout of BQ are corresponding to trace CEA, resulting in the highly electrochemical reduction signal. Under the optimal conditions, the linear range of CEA concentration was 0.0001-100 ng mL-1, and the limit of detection (LOD) could be as low as 0.05 pg mL-1. Importantly, the immunosensor also showed acceptable stability, reproducibility and selectivity.

Multiplexed electrochemical aptasensor based on mixed valence Ce(III, IV)-MOF for simultaneous determination of malathion and chlorpyrifos.

In this work, a multiplexed electrochemical aptasensor based on mixed valence Ce-MOF was constructed for the simultaneous determination of malathion and chlorpyrifos. Firstly, Ce(III, IV)-MOF materials with many catalytic sites were synthesized and characterized by SEM, TEM, XPS, FT-IR, XRD, and UV-Vis. Then, the chlorpyrifos and malathion signal markers based on Ce(III, IV)-MOF were prepared using thionine (Thi) and ferrocene (Fc) used as the electrochemical probe. The electrochemical signal was amplified by the reduction of thionine catalyzed by the spontaneous cycle of Ce(III, IV) in Ce(III, IV)-MOF skeleton and the reduction of ferrocene catalyzed by ascorbic acid (AA) in solution. The detection of the two targets did not interfere with each other, and the quantitative detection was realized with high sensitivity. The detection range of chlorpyrifos and malathion were 1.0 µM ∼ 0.1 pM, and the detection limits of chlorpyrifos and malathion were 0.038 and 0.045 pM (S/N = 3), respectively. The sensor provided a new idea for the simultaneous determination of multi-component and had a high application prospect in the field of food safety in the future.

A Novel Frequency Stabilization Approach for Mass Detection in Nonlinear Mechanically Coupled Resonant Sensors.

Frequency stabilization can overcome the dependence of resonance frequency on amplitude in nonlinear microelectromechanical systems, which is potentially useful in nonlinear mass sensor. In this paper, the physical conditions for frequency stabilization are presented theoretically, and the influence of system parameters on frequency stabilization is analyzed. Firstly, a nonlinear mechanically coupled resonant structure is designed with a nonlinear force composed of a pair of bias voltages and an alternating current (AC) harmonic load. We study coupled-mode vibration and derive the expression of resonance frequency in the nonlinear regime by utilizing perturbation and bifurcation analysis. It is found that improving the quality factor of the system is crucial to realize the frequency stabilization. Typically, stochastic dynamic equation is introduced to prove that the coupled resonant structure can overcome the influence of voltage fluctuation on resonance frequency and improve the robustness of the sensor. In addition, a novel parameter identification method is proposed by using frequency stabilization and bifurcation jumping, which effectively avoids resonance frequency shifts caused by driving voltage. Finally, numerical studies are introduced to verify the mass detection method. The results in this paper can be used to guide the design of a nonlinear sensor.

A label-free electrochemical aptasensor based on 3D porous CS/rGO/GCE for acetamiprid residue detection.

A novel label-free electrochemical aptasensor was fabricated based on a three-dimensional porous electrode (3D-CS/rGO/GCE) for the detection of acetamiprid residues. The sensing signal was generated by the DNA itself. The porous electrode was prepared by electrodeposition in situ and characterized by scanning electron microscope (SEM), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). These results indicated that the porous electrode has a uniform nanoporous structure, high active area, and excellent conductivity, leading to improve the transmission efficiency of current signals. The 3D-CS/rGO/GCE was used to increase a load of acetamiprid aptamer on the electrode. Meanwhile, DNA self-assembly strategy was used to further increase the DNA amounts. Thus the electrochemical current was amplified significantly due to increased phosphate group amounts by the above synergistic effect. The determination of acetamiprid residues using square wave voltammetry (SWV) showed good sensitivity, with the linear range from 0.1 pM to 0.1 µM and the detection limit was 71.2 fM. The label-free electrochemical aptasensor was also used to detect acetamiprid residues in tea samples with satisfactory results.