Provided are a cell imaging device and a cell imaging method that can shorten the time period of taking images of cells in a liquid sample, compared with conventional techniques. This cell imaging device introduces a urine sample containing cells into an internal space of a sample cell, moves at least one of the sample cell and an objective lens in a second direction while at least one of the sample cell and the objective lens is moved in a first direction, the second direction being different from the first direction, and takes, at a plurality of imaging positions, images of cells contained in the urine sample by means of an imaging unit.

Systems for collecting light (e.g., in a flow stream) are described. Light collection systems according to embodiments include: a mount having an orifice for receiving light, an adapter configured for attaching a camera to the mount and a fastener for attaching a lens to the distal end of the mount and a releasably attachable connecter that is configured for coupling to an orifice plate and an aligner that is configured to couple with an aligner on the mount and maintain optical alignment between the mount and connector. Methods for coupling a connector and a mount are also described. Systems and methods for measuring light emitted by a sample (e.g., in a flow stream) are also provided.

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.

A method and system are provided for focusing an imaging device on a liquid sample flowing through a field of view of the imaging device. Objects are segmented in the captured frames and used to account for the fact that the sample is flowing. Object velocities are calculated and used in selecting an appropriate focus value. The calculation of a focus measure takes account of the number of objects in captured frames in order to ensure a consistent calculation of the focus measure.

An improved optical flow cell adapted for use in a flow cytometer for differentiating formed bodies (e.g., blood cells) in liquid suspensions. Preferably manufactured by assembling, aligning, and optically joining at least two elements made from transparent material, the improved flow cell has a seamless internal flow channel of preferably non-circular cross-section in a cylindrical first element through which prepared samples can be metered and an independent second element having an external envelope suited to acquisition of optical parameters from formed bodies in such suspensions, the second element being conforming and alignable to the first element so that non-axisymmetric refractive effects on optical characterizing parameters of formed bodies passing through the flow channel in the first element may be minimized before the two elements are optically joined and fixed in working spatial relationship.

A method of analyzing a sample receiving a particle of interest, including: defining a reference point located on a first interface of the sample, or at a known distance from the sample, along the optical axis of the optical system; acquiring a reference image transmission of the sample, the object plane of the optical system being located at a known distance from the reference point along an axis parallel to the optical axis of the optical system, and the particle of interest being located outside of the object plane; using the reference image, digitally constructing a series of reconstructed images, each associated with a predetermined offset of the object plane along the optical axis of the optical system; and using the series of reconstructed images, determining the distance along an axis parallel to the optical axis of the optical system, between the particle of interest and the reference point.

Provided are microfluidic systems and methods for detecting, sorting, and dispensing of low abundance events such as single cells and particles, including a variety of eukaryotic and bacterial cells, for a variety of bioassay applications. The systems and methods described herein, when implemented in whole or in part, will make relevant microfluidic based tools available for a variety of applications in biotechnology including antibody discovery, immuno-therapeutic discovery, high-throughput single cell analysis, target-specific compound screening, and synthetic biology screening.

The inventive concept discloses a time series quantification method of supravital dye uptake of a cell using a lens-free imaging system.

An optical proximity sensor includes a first vertical cavity surface-emitting laser configured for self-mixing interferometry to determine distance to and/or velocity of an object. The optical proximity sensor also includes a second vertical cavity surface-emitting laser configured for self-mixing interferometry to determine whether any variation in a fixed distance has occurred. The optical proximity sensor leverages output from the second vertical cavity surface-emitting laser to calibrate output from the second vertical cavity surface-emitting laser to eliminate and/or mitigate environmental effects, such as temperature changes.

This disclosure relates to configurable particle analyzer apparatuses and methods. In some embodiments, a modular particle analyzer includes a stray light blocking module including a focusing lens, a pinhole, and a collimating lens. The focusing lens is configured to focus light emitted from the flowcell through the pinhole. The pinhole is configured to block stray or scattered light emitted from the flowcell. The collimating lens is configured to substantially collimate the light exiting the pinhole to output a substantially collimated light beam. A modular particle analyzer may alternatively, or additionally, include a rod-and-cage architecture. A particle analyzer may alternatively, or additionally, include a sheath pressure control module and a sample pressure control module. Further, a particle analyzer may alternatively, or additionally, include a sample probe wash. Any of the embodiments described herein may be combined with any one or more of the other embodiments described herein.