Electrochemical DNA biosensors based on long-range electron transfer: investigating the efficiency of a fluidic channel microelectrode compared to an ultramicroelectrode in a two-electrode setup.

Here, we describe the transposition of an ultramicroelectrode (UME) setup into a microfluidic chip configuration for DNA biosensors. The hydrodynamic properties of the fluidic channel microelectrode were screened with an [Fe(iii)(CN)6]3-/[Fe(ii)(CN)6]4- redox couple by cyclic voltammetry to provide a basis for further biological processes. A 23-base DNA probe was self-assembled into a monolayer on gold microelectrodes both in classical configuration and integrated in a microfluidic setup. Special interest was focused on the DNA target mimicking the liver-specific micro-ribonucleic acid 122 (miRNA122). Long-range electron transfer was chosen for transducing the hybridization. This direct transduction was indeed significantly enhanced after hybridization due to DNA-duplex π-stacking and the use of redox methylene blue as a DNA intercalator. Quantification of the target was deduced from the resulting electrical signal characterized by cyclic voltammetry. The limit of detection for DNA hybridization was 0.1 fM in stopped flow experiments, where it can reach 1 aM over a 0.5 µL s-1 flow rate, a value 104-fold lower than the one measured with a conventional UME dipped into an electrolyte droplet under the same analytical conditions. An explanation was that forced convection drives more biomolecules to the area of detection even if a balance between the speed of collection and the number of biomolecules collected has been found. The latter point is discussed here along with an attempt to explain why the sensor has reached such an unexpected value for the limit of detection.

Electrical impedance spectroscopy of a PET chip sandwiched between two disk electrodes: understanding the contribution of the polymer/electrode interface.

This work is devoted to the understanding of the dielectric impedance response of a semi-crystalline polyethylene terephthalate (PET) membrane sandwiched between two disk electrodes under alternate voltage excitation in the frequency range between 1 MHz and 25 mHz. Experimental results obtained for various PET thicknesses (36, 50 and 100 µm) highlighted the influence of the contact resistance at the electrode/polymer interface. For a better understanding of the PET/electrode interface behaviour, the experiments were compared with simulations performed for three different descriptions: the direct use of electrical equivalent circuits, an analytical model accounting for a power-law distribution of resistivity, and a numerical model (finite element simulations of the whole cell). The results highlight that the resistivity distribution obtained using the power-law model provided an appropriate description of the system in the frequency range investigated while the use of the CPE model is only consistent for low-frequencies (below 1 Hz).

Nanowires network for biomolecular detection using contactless impedance tomoscopy technique.

Here we present the detection of ultralow concentrations of biomolecules in a device made from a polycarbonate membrane containing a network of gold nanowires and using a "contactless" impedance tomoscopy technique. The sensor comprises a thin dielectric layer with two parallel band electrodes on the one side and a microchannel containing gold nanowires onto which the adsorption of antibodies occurs. Upon applying a high-frequency ac voltage between the two electrodes, the adsorption process occurring at the surface of the gold nanowires can be followed through contactless impedance measurements. The configuration allows the real-time detection of biomolecules with a bulk concentration in the picomolar range.