A tip for use in an optical detection system to analyze an analyte in a fluid sample drawn into the tip, using light reflected from a detection surface inside the tip that the analyte binds to, comprising a first detection surface and a second detection surface located in a same flow path with no controllable valve separating them, wherein the first and second detection surfaces have different surface chemistries.

A sensor device includes a flow path and a metal layer disposed in the flow path. The flow path is configured to allow a sample containing analytes to flow and to allow a carrier to be disposed therein. The carrier has acceptors that are fixed on a surface thereof and specifically bound with the analytes for producing aggregates. The flow path includes an aggregate trapping section at which the analytes locally concentrate to the section. This sensor device has high detection sensitivity with a simple structure.

A sensor arrangement performs simultaneous measurement of optical and electrical properties of a dielectric medium to be investigated, as well as the analytes contained therein. The arrangement contains a field-effect transistor and a surface plasmon resonance sensor. The sensor arrangement further contains a sample chamber for receiving the dielectric medium, which sample chamber is arranged such that the optical and electrical properties of the dielectric medium can be recorded simultaneously. The gate electrode of the field-effect transistor forms the active surface and/or is connected to the active surface of the surface plasmon resonance sensor, and has charge carriers which can be caused to oscillate by use of electromagnetic radiation.

The presence of hemozoin as an indicator of malaria in a blood sample is detected by magnetic separation, dissolution and spectroscopic analysis.

Supplying a liquid to a detection chip including a housing having an opening portion and internally housing the liquid and including an elastic sheet covering the opening portion and having a penetrating portion providing communicating between the inside and the outside of the housing, specifically by inserting a liquid delivery nozzle to the housing via the penetrating portion and supplying the liquid into the housing in a state where the nozzle is in contact with the elastic sheet so as to close the penetrating portion. The penetrating portion is one of a hole and a notch. One of the maximum length of the opening of the hole and the maximum length of the notch is smaller than the outer diameter of the nozzle at a portion coming in contact with the elastic sheet when the nozzle is inserted to close the penetrating portion when a liquid is supplied into the housing.

A graphene optical sensor includes a graphene layer having a surface, a first electrode and a second electrode, formed on the surface of the graphene layer, and arranged in a first direction parallel to the surface of the graphene layer, and a plurality of plasmonic antennas provided on the surface of the graphene layer between the first and second electrodes. Each plasmonic antenna of the plurality of plasmonic antennas, in a plan view, includes a first rod portion extending in a second direction inclined from the first direction, and a second rod portion extending in a third direction inclined from the first direction in a direction opposite the second direction with reference to the first direction, and intersecting the first rod portion. The plurality of the plasmonic antennas is arranged periodically in the second direction and in the third direction.

A system and method for evaluation of an interaction between an analyte in a fluid sample and a ligand immobilized on a sensor surface of a biosensor is provided. In one example, the system includes a plurality of needles, each being arranged to inject a fluid sample to one of sensor surfaces or detection spots. A plurality of fluid samples, each containing known concentrations of analyte, is provided. The plurality of fluid samples may be divided into at least two groups, each group having a number of fluid samples corresponding to the number of needles. The system and method is configured to perform the injections without intermediate regeneration or renewal of the immobilized ligand. Software for performing the steps of the method and a computer readable medium for storing the software are also provided.

A gas detector (10) includes a cell internal space (130) into which a target gas is supplied, the target gas exhibiting an absorption peak in an absorption spectrum; a light source (410) configured to generate light having at least a wavelength belonging to the absorption peak; and a photodetector (420) configured to detect the light that has emitted from the light source (410) and has propagated through the cell internal space (130). The gas detector (10) further includes a conductive thin film (220) in which a plurality of optical apertures (222) are regularly arranged such that a transmission peak in a transmission spectrum is superimposed over the absorption peak in the absorption spectrum along a wavelength axis. The conductive thin film (220) is provided on an optical path extending from the light source (410) to the photodetector (420), and is provided so as to be contactable with the target gas within the cell internal space (130).

A micro-fluidic chip comprises a chip base, a hemispherical or curved lens, and a securing portion. The chip base has a flow cell and a micro-fluidic channel defined therein. The micro-fluidic channel is fluidly connected to the flow cell to deliver fluid to and from the flow cell, respectively via a fluid input port and a fluid output port. The lens has an apex and a base. The apex is positioned within the flow cell. The securing portion is affixed to the chip base such that the lens is sandwiched between the chip base and the securing portion. The securing portion has a circular cavity defined therein in a surface adjacent the chip base, for receiving the base of the lens. The securing portion further has separate light input and output channels to allow light in and out, respectively, of the circular cavity and the lens.

A disposable micro-prism test chip for surface plasmon resonance measurement comprises a micro-tray and a micro-prism mounted on the micro-tray. The micro-tray and the micro-prism form at least one cell for providing a fluid dielectric medium for measurement. The disposable micro-prism test chip also comprises a thin metal layer coated on the surface of the micro-prism in the formed cell between the fluid dielectric medium and the micro-prism. The micro-tray may have at least one through window for forming the at least one cell. The micro-tray may also have a half-through cavity facing the micro-prism. The disposable micro-prism test chip is disposed after at least one use. The micro-prism may be fabricated by pulling a heated preform, where the preform has the same cross-section as that of the pulled micro-prism.