A reference body 1 includes: a support 10 provided with a first light passing portion 18, a second light passing portion 19, a first accommodating space 14, and a second accommodating space 15; a first fluorescent body 20 accommodated in the first accommodating space 14 and configured to emit first fluorescence in a second wavelength band when irradiated with first excitation light in a first wavelength band through the first light passing portion 18; a second fluorescent body 30 accommodated in the second accommodating space 15 and configured to emit second fluorescence in the second wavelength band when irradiated with second excitation light in the first wavelength band through the second light passing portion 19; and a light shielding portion 13 disposed between the first accommodating space 14 and the second accommodating space 15. In a case where a light amount of the first excitation light incident on the first light passing portion 18 and a light amount of the second excitation light incident on the second light passing portion 19 are equal to each other, a light amount of the first fluorescence emitted from the first light passing portion 18 and a light amount of the second fluorescence emitted from the second light passing portion 19 are different from each other.

A device for determining an assay result may include a test strip, a light source system, a light detection system, and a processor.

There is provided a test method for analyzing a body fluid in which a test tape is used in a test device to successively provide analytical test fields stored on the test tape, wherein body fluid is applied by a user to the test field provided at a time and the said test field is photometrically scanned using a measuring unit of the device to record measurement signals. To increase the measurement reliability, it is proposed that a control value is determined from a time-dependent and/or wavelength-dependent change in the measurement signals and that the measurement signals are processed as valid or discarded as erroneous depending on the control value.

The present disclosure relates to a surface-enhanced Raman scattering (SERS) lateral flow immunoassay strip containing: a sample pad into which a sample containing a target material is introduced; a conjugate pad containing a hollow metal nanoprobe for surface-enhanced Raman scattering, on which an antibody that can be coupled to the target material and a Raman marker are immobilized; and a detection pad including a detection region to which a secondary antibody that can be coupled to the target material coupled to the hollow metal nanoprobe is immobilized. Use of the SERS-based lateral flow immunoassay strip according to the present disclosure enables high-sensitivity quantitative analysis and qualitative analysis of the target material from Raman signal measurement depending on the concentration of the target material.

A reflectometer and method of use for measuring an amount of analyte in a sample are provided. The reflectometer can include a plurality of reading heads for obtaining reflectance information from discrete regions on a lateral flow test strip. The reflectance information is processed to obtain a digital value for the reflectance. The discrete regions can include a test zone and at least two control zones that each has a differing amount of detection moiety binding substance. The digital values for each control zone can be employed to establish a high end standard and a low end standard. The digital value for the test zone interpolated to the standards to obtain an accurate quantitative value for the analyte in the sample.

A cassette is disclosed that permits, with an instrument, quantitative analysis to be performed at the moment of sample testing without additional steps to the end user. The cassette includes a calibration strip and a sample strip. The calibration strip contains known quantities of analyte, from which a calibration curve can be created and applied to the analysis of the sample strip. The disclosed cassette can utilize light transmission or light reflectance techniques. The cassette may include a separate wash port for rapid washing of a high background sample. The disclosed cassette may perform diagnostic tests for humans, animals, environmental sample, and/or food samples. In some cases, the disclosed devices and techniques may be used to monitor efficacy of drug therapy and patient compliance with respect to physician-prescribed medication in a point of care setting.

A computer system and method is provided to filter clearance sensor data output by a sensor system during a load/offload procedure of a first object relative to a second object. A processing device of the computer system is configured to access hard threshold data, unique threshold data, and sensor data output by the sensor system sensing aspects of the load/offload procedure. The processing device is further configured to determine whether the sensor data exceeds the unique threshold, determine whether the sensor data that is determined to exceed the unique threshold is voidable data related to a noncritical event, and generate filtered sensor data that includes modifications to the voidable data.

An improved optical detection unit for an assay device, such as a lateral flow device, for the quantitative determination of the concentration of an analyte in a liquid sample, and an assay device comprising the same. The detection unit comprises an organic light emitting diode (OLED) emitter that has an emission spectrum E within the wavelength range from ?1 to ?2, and an organic photodiode detector (OPD) that has a light detection spectrum S within the wavelength range from ?1 to ?2. The detection unit has a test region that comprises a light absorbing component that has an absorbance spectrum A within the wavelength range from ?1 to ?2. The test region is positioned adjacent to the emitter and the detector to form an optical pathway from the light emitting diode to the photodiode through at least a portion of the test region. Formula M defines a relationship between E, S and A, and M is less than about 0.4.

An immunochromatography for multi-item detection is provided which contains detecting and measuring fluorescence and light absorption respectively at once with a detection device. The immunochromatography contains using fluorescent particles and light absorbing particles, wherein the fluorescence excitation wavelength of the fluorescent particles and the absorption wavelength of the light absorbing particles are in the same wavelength region; and detecting and measuring, at once, the intensity of reflected light from a test area, the intensity of reflected light from another test area, and the intensity of reflected light from a non-test area other than the test areas.

A device for determining an assay result may include a test strip, a light source system, a light detection system, and a processor.