The present disclosure describes a Lambertian gas-sensing system that may enable gas sensing in a compact form factor. The Lambertian gas-sensing system may include a hollow cavity, one or more light-emitting diode (LED) illuminators, one or more light-absorption detectors, and a gas exchange manifold. The hollow cavity may mechanically integrate the gas exchange manifold, the one or more LED illuminators, and one or more light-absorption detectors (such as one or more optical detectors). The gas exchange manifold may introduce gas into the hollow cavity and the one or more LED illuminators may emit light into the hollow cavity through one or more ports. The one or more light-absorption detectors may receive light from the hollow cavity through one or more ports.

A cuvette for analysis of liquids, including a first cuvette portion and a second cuvette portion, which are joined together, with a cuvette cavity, an inlet passage and an outlet passage being formed between the first cuvette portion and the second cuvette portion, the inlet passage and the outlet passage both in communication with the cuvette cavity, wherein the outlet passage is provided therein with a labyrinth-like sealing structure, which prevents backfill of a gas that has been discharged from the outlet passage during filling of a liquid to be analyzed in the cuvette.

A cuvette for analysis of liquids, including a first cuvette portion and a second cuvette portion, which are joined together, with a cuvette cavity, an inlet passage and an outlet passage being formed between the first cuvette portion and the second cuvette portion, the inlet passage and the outlet passage both in communication with the cuvette cavity, wherein the outlet passage is provided therein with a labyrinth-like sealing structure, which prevents backfill of a gas that has been discharged from the outlet passage during filling of a liquid to be analyzed in the cuvette.

A method for determining an optical pathlength through a cuvette of a spectrophotometric apparatus includes obtaining a first single beam spectrum of a liquid zero-material at least in a first energy region in which the liquid zero-material absorbs at least a portion of incident optical radiation; obtaining a second single beam spectrum of a second liquid at least in the first energy region, the second liquid having a composition excluding the liquid zero-material and having no absorption of incident optical radiation in the first energy region; determining a dual beam spectrum of the liquid zero-material relative to the second liquid at least in the first energy region from the first and second single beam spectra; and calculating an optical pathlength through the cuvette based on processing spectral information obtained from the first energy region of the determined dual beam spectrum.

The biometric system comprises: a measurement cartridge; and a meter, equipped with the measurement cartridge, for measuring an analyte present in a sample of the measurement cartridge. The measurement cartridge comprises a reagent container, a capillary module, and a reagent rod. The reagent container receives a liquid reagent and has a top sealed with a sealing film. The capillary module comprises a capillary tube which is located on an upper side of the reagent container and collects the sample by a capillary phenomenon, and the capillary tube is introduced into the reagent container by rupturing a contact portion to the sealing film by an applied pressure.

The biometric system comprises: a measurement cartridge; and a meter, equipped with the measurement cartridge, for measuring an analyte present in a sample of the measurement cartridge. The measurement cartridge comprises a reagent container, a capillary module, and a reagent rod. The reagent container receives a liquid reagent and has a top sealed with a sealing film. The capillary module comprises a capillary tube which is located on an upper side of the reagent container and collects the sample by a capillary phenomenon, and the capillary tube is introduced into the reagent container by rupturing a contact portion to the sealing film by an applied pressure.

A system for testing biological samples includes a frame having first and second sides and an aperture extending through the frame from the first side to the second side. First and second covers are attached to the first and second sides of the frame to form a well bounded by the frame, the first cover, and the second cover. An electromagnetic imaging device is used to image the biological sample through the first cover. A method is also conceived, wherein a first fluid is supplied to the well, the first fluid including live cells. A biofilm is grown from the live cells. A second fluid is supplied to the well and the biofilm is imaged using the electromagnetic imaging device.

The present disclosure describes a sample cell, method, and a computer implemented method of characterizing particles via an analytical flow field. In an exemplary embodiment, the sample cell includes (1) a sample cuvette including a top sample membrane, a sample container to contain a sample, and a bottom sample membrane, (2) a reference cuvette including a top reference membrane, a reference container to contain a solvent, and a bottom reference membrane, (3) where the sample cell is configured to allow a concentration boundary to form within the sample cell, and (4) where the sample cell is configured to allow the concentration boundary to move toward a bottom of the sample cell until equilibrium is reached in the sample cell.

The present disclosure describes a sample cell, method, and a computer implemented method of characterizing particles via an analytical flow field. In an exemplary embodiment, the sample cell includes (1) a sample cuvette including a top sample membrane, a sample container to contain a sample, and a bottom sample membrane, (2) a reference cuvette including a top reference membrane, a reference container to contain a solvent, and a bottom reference membrane, (3) where the sample cell is configured to allow a concentration boundary to form within the sample cell, and (4) where the sample cell is configured to allow the concentration boundary to move toward a bottom of the sample cell until equilibrium is reached in the sample cell.

An embodiment provides a nozzle, including: a conical-shaped portion having a first end and a second end substantially opposite the first end, wherein the first end has a smaller diameter than the second end; the first end having an attachment to hold the nozzle in a flow of fluid from an inlet, wherein the nozzle is positioned with the first end facing an inflow of a fluid and the second end facing a chamber; and the conical-shaped portion configured to direct the inflow of the fluid along an inner surface of the chamber, wherein the inflow of the fluid travels around the outer diameter of the conical-shaped portion. Other aspects are described and claimed.