ABSTRACT
Magnetic sensor systems integrate a sensing element and magnetic field generators to determine their relative position or to measure movement. Typically, the magnetic fields are produced by permanent magnets, which have high intensity but are hard to machine into custom shapes. However, novel solutions using magnetic polymer composites (MPCs) have emerged as field generators due to their low cost, weight and patterning freedom. Here, we present a finite element model developed in COMSOL Multiphysics that allows the design of complex magnetization patterns on these polymer composites, taking into account the geometries of the parts and the magnetic properties of the materials employed. The model, together with the characterization protocol of the materials, has proved to be capable of predicting the magnetization of polymer composites at different temperatures. In addition, the model incorporates the properties of the magnets used during the magnetization process, such as the size, shape and magnetization, as well as the properties of the surrounding elements. This new model facilitates the design of new polymeric parts with complex shapes and magnetization patterns that can be employed as field generators in magnetic sensing systems.
ABSTRACT
MicroRNAs (miRNAs) are biomarkers involved in biological processes that are released by cells and found in biological fluids such as blood. The development of nucleic acid-based biosensors has significantly increased in the past 10 years because the detection of such nucleic acids can easily be applied in the field of early diagnosis. These biosensors need to be sensitive, specific, and fast in order to be effective. This work introduces a newly-built electrochemical biosensor that enables a fast detection in 30 min and, as a result of its integration in microfluidics, presents a limit of detection as low as 1 aM. The litterature concerning the specificity of electrochemical biosensors includes several studies that report one base-mismatch, with the base-mismatch located in the middle of the strand. We report an electrochemical nucleic acid biosensor integrated into a microfluidic chip, allowing for a one-base-mismatch specificity independently from the location of the mismatch in the strand. This specificity was improved using a solution of methylene blue, making it possible to discriminate a partial hybridization from a complete and complementary hybridization.
ABSTRACT
In this article, we present the design, fabrication and characterization of a microfluidic device and a dedicated electronic system to perform 8 multiplexed electrochemical measurements of synthetic miRNA strands, as well as the biochemical protocols developed for the functionalization of the electrodes and the quantification experiments. The outcomes of this work highlight that the parallelization of eight microchannels containing 2-electrode cells driven by the dedicated electronics offers a solution as robust as a conventional 3-electrode cell and commercially available potentiostats. In addition, this solution presents the advantage of simultaneously reduce the microfabrication complexity, as well as offering an integrated; multiplexed and portable system for the quantification of miRNA. The results presented demonstrate that the system shows a linear response on concentrations down to 10-18 mol/L of perfect matched reporter and capture sequences of synthetic miRNA.
