A photoacoustic flow cytometry (PAFC) device for the in vivo detection of cells circulating in blood or lymphatic vessels is described. Ultrasound transducers attached to the skin of an organism detect the photoacoustic ultrasound waves emitted by target objects in response to their illumination by at least one pulse of laser energy delivered using at least one wavelength. The wavelengths of the laser light pulse may be varied to optimize the absorption of the laser energy by the target object. Target objects detected by the device may be unlabelled biological cells or cell products, contrast agents, or biological cells labeled with one or more contrast agents.

A device and method of using the device to detect the presence and composition of clots and other target objects in a circulatory vessel of a living subject is described. In particular, devices and methods of detecting the presence and composition of clots and other target objects in a circulatory vessel of a living subject using in vivo photoacoustic flow cytometry techniques is described.

To provide a technique capable of stably forming droplets.

There is provided a microparticle sorting device and the like including: an imaging element configured to acquire an image of fluid and a droplet at a position where liquid discharged from an orifice that generates a stream of the fluid is converted into a droplet; and a processing unit configured to determine a harmonic superposition amplitude ratio, a harmonic phase difference, and a superimposed wave voltage on the basis of states of a satellite droplet and a break-off point in the image.

A cytometer includes an avalanche photodiode, a switching power supply, a filter, and voltage adjustment circuitry. The switching power supply includes a feedback loop. The filter is electrically connected between the switching power supply and the avalanche photodiode. The voltage adjustment circuitry adjusts a voltage on the feedback loop based at least in part on a voltage measured between the filter and the avalanche photodiode.

Described herein are apparatuses and methods for analyzing an optical signal decay. In some embodiments, an apparatus includes: a source of a beam of pulsed optical energy; a sample holder configured to expose a sample to the beam; a detector comprising a number of spectral detection channels configured to convert the optical signals into respective electrical signals; and a signal processing module configured to perform a method. In some embodiments, the method includes: receiving the electrical signals from the detector; mathematically combining individual decay curves in the electrical signals into a supercurve, the supercurve comprising a number of components, each component having a time constant and a relative contribution to the supercurve; and quantifying a relative contribution of each component to the supercurve.

There is provided a fine-particle sorting apparatus, including: a determination unit that performs sorting determination of a particle, the determination unit performing the determination using rule data defining, in accordance with a particle population to which a particle that is a sorting-determination target belongs and a particle population to which a different particle within a predetermined range around the particle belongs, a relationship between the particles, particle populations to which the particle that is a sorting-determination target and the different particle within the predetermined range may belong including the following particle populations of (a) a particle population of particles to be sorted, (b) a particle population of particles that are not to be sorted but are ignorable in the determination, and (c) a particle population of particles that are neither the particles to be sorted nor the ignorable particles, the ignorable particles including red blood cells.

Provided are a cell sorting chip, device, and method based on dielectrophoresis induced deterministic lateral displacement, the chip including a microfluidic channel (4), the microfluidic channel comprising a sample inlet (4.1), a straight channel, and two sample outlets; three groups of electrode array pairs are integrated at a bottom of the straight channel, the three electrode array pairs respectively being a focusing electrode group (1), a sorting electrode group (2), and a separating electrode group (3); the focusing electrode group is used for cell focusing and signal detection; the sorting electrode group is used for single cell sorting; and the separating electrode group is used for single cell separation. High-speed, precise, and lossless target cell sorting can thus be implemented.

[Object] To provide an information processing apparatus, an information processing method, a program, and an observation system with which images of cells under observation are efficiently captured. [Solving Means] An information processing apparatus according to the present technology includes an image-capture controller unit, an image-capture area classifier unit, and an observation controller unit. The image-capture controller unit controls an image-capture mechanism to capture images of a culture vessel including a plurality of wells that house cells for each image-capture area. The image-capture area classifier unit applies image processing to the images captured by the image-capture mechanism and classifies the plurality of image-capture areas into a first image-capture area of which image-capturing is continued and a second image-capture area of which image-capturing is not continued on the basis of a result of the image processing. The observation controller unit instructs the image-capture controller unit to capture an image of an image-capture area classified as the first image-capture area and not to capture an image of an image-capture area as the second image-capture area.

Embodiments of the present invention encompass systems and methods for determining detection limits for various antibody-dye conjugates for flow cytometry. Exemplary techniques involve a linear superpositioning approach of spillover-induced enlargements of normally distributed measurement errors.

Provided herein are systems and methods of optical particle counters which account and adjust for the refractive index of the carrier fluid being analyzed. The provided systems are robust and may be implemented in a variety of optical particle counters including obscured light, reflected light, emitted light and scattered light particle counters. The described systems may be useful with any fluid, including gases or liquids. In some cases, the system can account for the differences in refractive index between two liquids, for example, ultrapure water and an acid, such as sulfuric, hydrochloric, hydrofluoric, acetic, phosphoric, chromic phosphoric, and the like. By accounting for the refractive index of the carrier fluid, the described systems and methods are also more sensitive and able to more accurately detect and characterize smaller particles, including nanoscale sized particles.