Described herein is a portable virometer for detecting viral targets. An exemplary virometer has a molecular electronics sensor with a first electrode, a second electrode spaced-apart from the first electrode by a nanogap, a bridge molecule having a first end and a second end, the first end coupled to the first electrode and the second end coupled to the second electrode, a hybridization probe having an oligonucleotide sequence from or related to a viral target is conjugated to the bridge molecule, a sample applicator for acquiring a sample and transferring it to the chip, and data processing software and hardware for providing a report of detection of viral targets. Methods of using the virometer for testing in the home, in schools, in workplaces, in hotels, in restaurants, or in public places are also described.

A nanobio-sensing device includes: a substrate; a source electrode and a drain electrode which are disposed on the substrate and spaced apart from each other; a sensing film which serves as a channel connecting the source electrode and the drain electrode and is in contact with at least a part of the source electrode and the drain electrode; a first gate electrode which is a floating gate, extends while one end of the first gate electrode is in contact with a part of the sensing film, and is capable of being in contact with a part of the source electrode and/or the drain electrode; and a second gate electrode which is in contact with the other end of the first gate electrode to form a first gate stacked structure.

In one embodiment, a sample surface of a biosensor includes pixel areas and holds a plurality of clusters during a sequence of sampling events such that the clusters are distributed unevenly over the pixel areas. In another embodiment, a biosensor has a sample surface that includes pixel areas and an array of wells overlying the pixel areas, the biosensor including two wells and two clusters per pixel area. The two wells per pixel area include a dominant well and a subordinate well. The dominant well has a larger cross section over the pixel area than the subordinate well. In yet another embodiment, an illumination system is coupled to a biosensor that illuminates the pixel areas with different angles of illumination during a sequence of sampling events, including, for a sampling event, illuminating each of the wells with off-axis illumination to produce asymmetrically illuminated well regions in each of the wells.

The present invention is related to engineered nucleic acid bases for use in molecular electronics, such as nanosensors, molecular-scale transistors, FET devices, molecular motors, logic and memory devices, and nanogap electronic measuring devices for the identification and/or sequencing of biopolymers.

Proposed is a quality analysis nanosensor using a metastructure, including: a metasurface structure resonating with a specific frequency of incident electromagnetic waves; a fixed binding body formed on a surface of the metasurface structure or inside the metasurface structure on a hotspot area; a movable binding body coupled to the fixed binding body by an attractive force; and a receptor or nanoparticles linked to the movable binding body. According to the nanosensor, there are provided a detection structure and method based on metamaterials and nanoparticles, thereby enabling efficient detection with only few nanoparticles by raising detection sensitivity to a high level.

A method for detecting a species of bacteria in a sample solution. The method includes putting the sample solution in contact with an array of zinc oxide nanorods on a gate region of a field effect transistor (FET) biosensor, applying an alternating current (AC) voltage between source and drain electrodes of the FET biosensor, applying a first direct current (DC) voltage of V.sub.1 to the sample solution, measuring a first set of electrical impedance values (Z.sub.1) between the source region and the drain region, calculating a first impedance difference set (ΔZ.sub.1) between the Z.sub.1 and a respective first initial set of electrical impedance values (Z.sub.1.sup.0) associated with a bacteria-free reference solution, determining bacteria indicative factors including a first impedance difference peak value (ΔZ.sub.1m) and a respective peak frequency (f.sub.m), and detecting a presence of a first species of bacteria in the sample solution based on the bacteria indicative factors.

A biosensor includes a source element; a drain element; a semiconductor channel element between the source element and the drain element for forming an electrically conductive channel with adjustable conductivity between the source and drain elements; a first gate element configured to be electrically biased to set a given operational regime of the sensor with given electrical conductivity of the channel; and a second gate element, physically separate from the first gate element, configured to contact a solution comprising analytes allowed to interact with a gate contact surface of the second gate element to generate a surface potential change dependent on the concentration of the analytes in the solution. The channel element is substantially fully depleted allowing the first and second gate elements to be electrostatically coupled such that the surface potential change at the second gate element is configured to modify the electrical conductivity of the channel.

A semiconductor sensor includes a substrate, a dielectric layer on the substrate, a first electrode on the dielectric layer, and a second electrode spaced apart from the first electrode and on the dielectric layer, a semiconductor sheet between the first electrode and the second electrode on the dielectric layer and electrically connecting the first electrode and the second electrode to each other, a third electrode at least a portion of which is covered by the dielectric layer and faces the semiconductor sheet with the dielectric layer interposed therebetween, and multiple first attraction portions at least on a surface of the third electrode or in or on the dielectric layer on the surface of the third electrode and attracting an object to be detected.

Devices for sequencing biopolymers and methods of using the devices are disclosed. In one example, such a device has a nanopore, a plurality of wells and fluidic tunnels to allow a biopolymer to translocate in the device. In some embodiments, the device may include integrated electronics or micro-electromechanical systems, such as valves, bubble generators/annihilators or pressure pulse generators, to actively control fluidic/ionic/electric flows in the device.

It is recognized that, because of its unique properties, graphene can serve as an interface with biological cells that communicate by an electrical impulse, or action potential. Responding to a sensed signal can be accomplished by coupling a graphene sensor to a low power digital electronic switch that is activatable by the sensed low power electrical signals. It is further recognized that low power devices such as tunneling diodes and TFETs are suitable for use in such biological applications in conjunction with graphene sensors. While tunneling diodes can be used in diagnostic applications, TFETs, which are three-terminal devices, further permit controlling the voltage on one cell according to signals received by other cells. Thus, by the use of a biological sensor system that includes graphene nanowire sensors coupled to a TFET, charge can be redistributed among different biological cells, potentially with therapeutic effects.