To provide a concentration measurement method with which the concentrations of predetermined chemical components can be measured non-destructively, accurately, and rapidly by a simple means, up to the concentrations in trace amount ranges, as well as a concentration measurement method with which the concentrations of chemical components in a measurement target can be accurately and rapidly measured in real time up to the concentrations in nano-order trace amount ranges, and which is endowed with a versatility that can be realized in a variety of embodiments and modes. In the present invention, a measurement target is irradiated, in a time sharing manner, with light of a first wavelength and light of a second wavelength that have different optical absorption rates with respect to the measurement target. The light of each wavelength, arriving optically via the measurement target as a result of irradiation with the light of each wavelength, is received at a shared light-receiving sensor. A differential signal is formed, the differential signal being of a signal pertaining to the light of the first wavelength and a signal pertaining to the light of the second wavelength, the signals outputted from the light-receiving sensor upon receipt of the light. The concentration of a chemical component in the measurement target is derived on the basis of the differential signal.

A tissue inflammation detection system (600) including: a light emitter (602) configured to emit light towards tissue (604); at least one light detector (606) configured to detect diffuse reflective light from the tissue; and a controller (613) including a tissue inflammation detection unit (614) configured to analyze the detected diffuse reflective light in its spectral components. The tissue inflammation detection unit is configured to: determine a tissue contribution from a first wavelength region of a diffuse reflective spectroscopy signal where the diffuse reflective spectroscopy signal is dominated by tissue; extrapolate the tissue contribution to a second wavelength region where the diffuse reflective spectroscopy signal includes at least one detectable hemoglobin absorption feature; subtract the extrapolated tissue contribution from the diffuse reflectance signal; and determine the degree of tissue inflammation.

A growth information management apparatus is provided, which can accurately ascertain a growth situation of plants or the like regardless of a positional change of an equipment where the apparatus is mounted. A growth information management apparatus 100 emits a measuring beam to a plant P and acquires growth information on the plant, based on received reflected light, with the growth information management apparatus being mounted on another equipment 1. The growth information is corrected based on change information on the irradiation direction of the measuring beam according to a positional change of the other equipment.

Devices, methods, systems, and computer-readable media for a dual wavelength source gas sensor are described herein. One or more embodiments include a gas sensor, comprising: a dual wavelength source to transmit a first wavelength and a second wavelength via an optical path, wherein a gas is present through the optical path, a detector to receive the first wavelength and the second wavelength via the optical path, and a computing device coupled to the detector to determine an determine a signal intensity for the first wavelength and the second wavelength.

This present invention relates generally to devices, systems, and methods for performing optical and electrochemical assays and, more particularly, to devices and systems having universal channel circuitry configured to perform optical and electrochemical assays, and methods of performing the optical and electrochemical assays using the universal channel circuitry. The universal channel circuitry is circuitry that has electronic switching capabilities such that any contact pin, and thus any sensor contact pad in a testing device, can be connected to one or more channels capable of taking on one or more measurement modes or configurations (e.g., an amperometric measurement mode or a current drive mode).

Analyzers and methods for making and using analyzers are described such as a method in which multiple absorption readings of a liquid assay are obtained by a photodetector using multiple light sources having at least three separate and independent wavelength ranges and with each of the absorption readings taken at a separate instant of time. Using at least one processor and calibration information of the liquid assay, an amount of at least two analytes within the liquid assay using the multiple absorption readings is determined.

A system for measuring the blood loss comprises a measuring device that determines a hemoglobin concentration of fluid within a container utilizing a light source and a light detector. The container receives blood and other fluids from a patient during a medical procedure. Light from the light source is passed through the blood and other fluids in the container and is detected by the light detector. Based upon a magnitude of light detected, a hemoglobin concentration of the fluid in the container can be determined. A volume-measuring device determines the volume of blood and fluid in the container. Knowing the hemoglobin concentration and volume of fluid in the container, the volume of patient blood loss in the container can be determined. The blood loss measuring device in combination with infusion systems maintains a real-blood volume status so that proper infusion of blood, crystalloid and/or colloid solutions occurs.

For determining concentration of a targeted molecule M in a liquid sample admixed with interfering molecules M.sub.J which overlap its absorption band, a NDIR reflection sampling technique is used. Besides the signal source, a reference and an interference source are added. M is calculated by electronics which use R.sub.ave(t) from a pulsed signal and reference channel output and a calibration curve which is validated by use of R.sub.Java(t.sub.2) from a pulsed interference and reference channel output. Signal, interference and reference sources are pulsed at a frequency which is sufficiently fast so that a given molecule of M or M.sub.J will not pass in and out of the liquid sampling matrix within the pulsing frequency.

A bilirubin concentration measurement system according to the present invention includes: a sensor device attachable to a subject; and a terminal device capable of wirelessly communicating with the sensor device. The sensor device includes: a light emitting element that emits blue light; a light emitting element that emits green light; a light detection element that detects reflected light that is the blue light having been incident on skin of the subject and been reflected, and detects reflected light that is the green light having been incident on the skin of the subject and been reflected; and a communication unit that wirelessly transmits information about intensities of the reflected light detected by the light detection element. The terminal device includes: a communication unit that receives the information about the intensities of the reflected light transmitted from the sensor device; and a computing unit that calculates a bilirubin concentration using the information about the intensities of the reflected light.

A blood coagulation analyzer comprises: a light irradiation unit configured to apply light onto a container configured to store a measurement specimen containing a sample and a reagent, and comprising: light sources including a first light source configured to generate light of a first wavelength for blood coagulation time measurement, a second light source configured to generate light of a second wavelength for synthetic substrate measurement, and a third light source configured to generate light of a third wavelength for immunonephelometry measurement; and optical fiber parts facing the respective light sources; a light reception part configured to receive light transmitted through the container; and an analysis unit configured to analyze the sample using an electric signal outputted from the light reception part.