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.

This invention provides new methods and apparatus for rapidly analyzing a single bioparticle or a plurality of bioparticles to assess their condition. The invention is enabled by an optical microcavity comprising reflective structures to confine light and bioparticles in the same space. Under resonance conditions, an electromagnetic standing wave is established in the microcavity to interact with the bioparticle. Means are provided to bring a bioparticle into the microcavity and to detect changes in the resonance condition with and without the bioparticle in the microcavity. Information about the bioparticle is obtained using the benefits of light interactions as fast, non-contacting, and non-destructive.

A microfluidic chip orients and isolates components in a sample fluid mixture by two step focusing, where sheath fluids compress the sample fluid mixture in a sample input channel in one direction, such that the sample fluid mixture becomes a narrower stream bounded by the sheath fluids, and by having the sheath fluids compress the sample fluid mixture in a second direction further downstream, such that the components are compressed and oriented in a selected direction to pass through an interrogation chamber in single file formation for identification and separation by various methods. The isolation mechanism utilizes external, stacked piezoelectric actuator assemblies disposed on a microfluidic chip holder, or piezoelectric actuator assemblies on-chip, so that the actuator assemblies are triggered by an electronic signal to actuate jet chambers on either side of the sample input channel, to jet selected components in the sample input channel into one of the output channels.

An apparatus for analyzing particles in a solution includes a unit configured to place a flow cell having a flow path for flowing a sample solution containing the particles; a unit configured to illuminate the sample solution flowing through the flow path of the flow cell; a photodetector that detects a scattered light and/or fluorescence generated from the particles in the sample solution; and a unit configured to analyze the particles based on their signal intensities detected by the photodetector, wherein the flow cell has the flow path formed in a substrate, a reflection plane is formed on the side surface of the flow path, the reflection plane leads the lights generated in the flow path of the flow cell and advancing in the substrate in-plane direction to a specified region of the surface of the flow cell, and the photodetector detects the light exiting from the specified region to the outside.

Provided is a biological sample imaging device and a biological sample imaging method that are capable of disposing a sufficient number of large-sized particles in a biological sample so as to be moderately dispersed within an imaging range. The biological sample imaging method includes: a first step of introducing a biological sample containing particles into a liquid flow channel; a second step of causing the biological sample introduced into the liquid flow channel to flow in a forward direction; a third step of causing the biological sample to flow in a reverse direction after the second step; and an imaging step of taking, in an imaging cell, images of the particles contained in the biological sample that remains in the liquid flow channel after the third step.

A microfabricated sheath flow structure for producing a sheath flow includes a primary sheath flow channel for conveying a sheath fluid, a sample inlet for injecting a sample into the sheath fluid in the primary sheath flow channel, a primary focusing region for focusing the sample within the sheath fluid and a secondary focusing region for providing additional focusing of the sample within the sheath fluid. The secondary focusing region may be formed by a flow channel intersecting the primary sheath flow channel to inject additional sheath fluid into the primary sheath flow channel from a selected direction. A sheath flow system may comprise a plurality of sheath flow structures operating in parallel on a microfluidic chip.

A particle detector, having a housing defining a chamber; an air stream injector, producing an airstream in said chamber from air taken from outside said chamber; a light source, producing a light beam that crosses the air stream and wherein said light beam is shaped so that a transverse extent of said light beam has a uniform intensity over said transverse extent of said air stream. Also, a photon detection assembly, including an optical train of lenses, is positioned to accept light from said light beam, emitted by the particles, and to focus this light onto a photon detector. A particle detection assembly detects the particles, responsive to the photon detection assembly. Finally, a particle size estimation assembly estimates size for each detected particle, based on number of photons detected by said photon detection assembly from said particle, as it crosses said light beam.

A compact flow instrument for multiplexed analysis of a pooled population of subsets of particles exposed to a sample includes an examination zone with one or more examination compartments for irradiating a passing particle with electromagnetic radiation (EMR), one or more EMR sources for irradiating the passing particle, one or more detectors configured to detect EMR emitted or scattered by the passing particle, a syringe pump driven by a stepper motor to deliver sheath fluid in characteristic pulses according to each step of the stepper motor for transporting the passing particle, and a controller. The controller is configured to actuate the syringe pump to deliver sheath fluid to transport the passing particle, capture the detected EMR at a rate commensurate with the velocity of the transported particle as it passes through the examination zone, and compile information about the captured EMR.

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.

A laser particle size analyzer with a liquid sheath flow measuring cell comprises a measuring cell which comprises a particle flow leading-in cavity (3000), a medium flow leading-in cavity (1000) and a measuring glass cavity (2000), wherein the medium flow leading-in cavity (1000) is connected to an upper portion of the measuring glass cavity (2000); the medium flow leading-in cavity (1000) is annularly arranged at a periphery of the particle flow leading-in cavity (3000), and a gap (607) is formed between the medium flow leading-in cavity (1000) and the particle flow leading-in cavity (3000); a medium flow (70) flows into the measuring glass cavity (2000) from the gap (607), and a particle flow (60) flows into the measuring glass cavity (2000) from the particle flow leading-in cavity (3000). The laser particle size analyzer achieves technical effects of long service life, simple operation and good use effect of the measuring cell.