A urine analyzer capable of operating in a urine measurement mode and a body fluid measurement mode, the urine analyzer includes a specimen preparing section configured to prepare a measurement specimen and a detecting section configured to derive signals of particles in the measurement specimen supplied from the specimen preparing section. A computer and a memory including programs on a computer-readable medium that enable the computer to execute operations to control the specimen preparing section and the detecting section in the urine measurement mode and in the body fluid measurement mode.

A sample measuring apparatus of an embodiment includes: a laser diode that applies laser light to a measurement specimen prepared from a sample; a detection unit that acquires optical information from a particle in the measurement specimen to which the laser light is applied; a drive circuit that supplies a direct-current drive signal to the laser diode; and a high-frequency conversion circuit that generates a potential that switches between a high level and a low level in a predetermined cycle to guide the drive signal outputted from the drive circuit to a second signal path which is different from a first signal path connected to the laser diode in the predetermined cycle, thereby converting the drive signal to be supplied to the laser diode into a high-frequency signal.

A system for characterizing at least one particle from a fluid sample is disclosed. The system includes a filter disposed upstream of an outlet, and a luminaire configured to illuminate the at least one particle at an oblique angle. An imaging device is configured to capture and process images of the illuminated at least one particle as it rests on the filter for characterizing the at least one particle. A system for characterizing at least one particle using bright field illumination is also disclosed. A method for characterizing particulates in a fluid sample using at least one of oblique angle and bright field illumination is also disclosed.

A testing method using a micro flow path device configured for a test liquid containing a specimen to be brought into contact with a drug therein and for a test on an action of the drug on the specimen includes: preparing the micro flow path device including: a plurality of micro flow paths, first and second openings which are disposed at both ends of each of the plurality of micro flow paths and communicate with an outside, a storage unit which is provided in each of the plurality of micro flow paths and stores the drug, and a gas-permeable membrane covering the first opening; applying a fluid pressure higher than an external pressure to the test liquid through the second opening from a syringe pump connected to the second opening to pressure-feed the test liquid to the storage unit; and observing a target region set in the micro flow path.

To provide a technology of maintaining light detection accuracy at a high level irrespective of individual variations in flow rate of microparticles flowing through a flow channel. The present technology provides a microparticle measuring apparatus including: a plurality of light detection sections configured to detect, at different positions, optical information emitted from microparticles flowing through a flow channel; and a detection timing control section configured to control a detection timing of each light detection section, on the basis of a trigger signal detected at a first reference channel provided in a first light detection section, and an optical signal detected at a second reference channel provided in a second light detection section that detects optical information emitted from the microparticles, at a position different from a position of the first light detection section.

A detecting device for detecting biological particles includes an optical system including an excitation light source, a filter and spectroscope group, a photomultiplier tube, and a charge-coupled device. The excitation light source illuminates the biological particles on a detecting carrier of the detecting device. A kind of target biological particles in the biological particles is excited to generate an emission light. The emission light enters the filter and spectroscope group to be separated into a first detecting light and a second detecting light. After the photomultiplier tube receives the first detecting light, the photomultiplier tube transmits a regional positioning signal to a processor of the detecting device. After the charge-coupled device receives the second detecting light, the charge-coupled device transmits an image signal to the processor. The processor obtains a precise location of the target biological particles based on the regional positioning signal and the image signal. A detecting method of the detecting device is also provided.

Stationary devices employing quadrature phase analysis light scattering are provided, to aid in the determination of the magnitude and polarity of electrophoretic mobility and zeta potential of particles in colloids. The devices use an optical quadrature interferometer with an electrophoresis sample chamber containing sample particles undergoing electrophoresis, the optical quadrature interferometer being configured to generate a quadrature signal. The phase of the quadrature signal may be analyzed at the frequency of the sample chamber electric field to estimate displacements and directions of the particles. The estimates can be used to determine a central value of the magnitude of the electrophoretic mobility, as well as its polarity. Particles having low electrophoretic mobility, or that may be adversely affected by high electric fields, can be analyzed, and constraints on vibration and light source coherence length may be relaxed. A phase modulator or frequency shifter is not required.

In one aspect, the present teachings provide a system for performing cytometry that can be operated in three operational modes. In one operational mode, a fluorescence image of a sample is obtained by exciting one or more fluorophore(s) present in the sample by an excitation beam formed as a superposition of a top-hat-shaped beam with a plurality of beams that are radiofrequency shifted relative to one another. In another operational mode, a sample can be illuminated successively over a time interval by a laser beam at a plurality of excitation frequencies in a scanning fashion. The fluorescence emission from the sample can be detected and analyzed, e.g., to generate a fluorescence image of the sample. In yet another operational mode, the system can be operated to illuminate a plurality of locations of a sample concurrently by a single excitation frequency, which can be generated, e.g., by shifting the central frequency of a laser beam by a radiofrequency. For example, a horizontal extent of the sample can be illuminated by a laser beam at a single excitation frequency. The detected fluorescence radiation can be used to analyze the fluorescence content of the sample, e.g., a cell/particle.

Systems and methods for imaging a plurality of blood fluid samples or other types of samples include processing at least a portion of a sample to enhance imageability of certain particles in that portion and subsequently imaging the sample portion. In some instances, processing and imaging of various samples may be staged in a manner to optimize throughput of the system or method.

[Object] To provide an information processing apparatus, a particle sorting system, a program, and a particle sorting method that practice a spectral type analysis usable for sorting particles.

[Solving Means] The information processing apparatus according to an aspect of the present technology includes: an analysis unit; a learning unit; and a discrimination unit. The analysis unit calculates fluorophore information indicating respective amounts of luminescence of a plurality of types of fluorophores on the basis of detection data indicating amounts of luminescence of fluorescence at respective wavelength bands, the fluorescence having been emitted from a particle irradiated with excitation light, discriminates whether or not to treat the particle as a process target in accordance with the fluorophore information, and generates teaching data by associating a result of the discrimination with the detection data. The learning unit applies a machine learning algorithm to the teaching data, learns a characteristic of the detection data discriminated as the process target, and generates dictionary data including a result of the learning. The discrimination unit discriminates whether or not the particle whose detection data has been acquired is the process target on the basis of the dictionary data when the detection data is supplied.