Provided are a liquid surface inspection device, an automated analysis device, and a liquid surface inspection method with which instances of contamination can be minimized and the accuracy of the manner in which the surface conditions, such as bubbles or the like, of a liquid substance are detected can be enhanced. The device has: a light illumination unit for illuminating a container holding a liquid substance, as well as the surface of the liquid substance, with light; an image capture unit for acquiring a video image having at least color information and brightness information of light from the container and the liquid substance which are illuminated by the light illumination unit; and a detection unit for using the color information and brightness information in the video image captured by the image capture unit to detect the condition of the liquid surface.

A treatment device (1) for treating histological or cytological samples has a plurality of containers (6) for different treatment agents and a detection apparatus (2) for detecting a code which unequivocally identifies a type of a treatment agent or a type of a group of treatment agents from a package or replacement container of a treatment agent or group of treatment agents. The device furthermore has an evaluation apparatus (18) that, based on a detected code, ascertains which of the containers is or are to be replenished or replaced, and an indicating apparatus (4) which communicates to a user the ascertained container (6) or containers (6) that is or are to be replenished or replaced. The indicating apparatus may include a display (5) presenting a schematic image of the plurality of containers (6) with image(s) of each ascertained container being marked, and/or a light source (15) that illuminates each ascertained container.

A two-dimensional code is attached to a location of a reagent storage unit which is visually recognizable from the outside, and a coordinate position of the two-dimensional code in a coordinate system of the two-dimensional code and coordinate information of an installation position of a reagent bottle are held. After that, an image of the two-dimensional code is captured by a portable terminal so that a coordinate system of an image capture unit of the portable terminal is converted into the coordinate system of the two-dimensional code using AR technology. The coordinate information of the installation position of the reagent bottle in the coordinate system of the two-dimensional code is regarded as positional coordinates in the captured image on the basis of the conversion, thereby ascertaining the position of the reagent bottle on the captured image and displaying the ascertained position on a display unit.

The automatic analyzer includes a light source 4a to perform measurement, a spectrophotometer 4, a reagent disk 9 to store a reagent bottle 10 in which the reagent is stored, a carriage device to carry the reagent bottle 10 to the reagent disk 9, a reagent preparation unit to perform preparatory operations required before the regent bottle 10 is used, and a control unit 21 to schedule the preparatory operations by the reagent preparation unit and the carriage operation by the carriage device such that the reagent bottle 10 is carried to the reagent disk 9 immediately after an operation accompanied with analysis by the light source 4a and the spectrophotometer 4 is suspended or ends.

The present invention relates to an improved abnormality determining method for an automatic analyzer and related automatic analyzer that detects abnormalities for a reaction process of a reaction solution. The method for determining the presence of absence of abnormalities in the reaction process and performs the determination by acquiring acquisition conditions for multiple items of measured data, acquiring the measured data detected by a spectral detector that match the acquisition conditions, calculating a feature quantity of the measured data, generating a determination criterion based on the feature quantity, and determining the presence or absence of abnormalities by comparing the feature quantity of the measured data subject to the determination with the determination criterion. The acquisition condition includes information relating to a number of a divisions of a measured value range and information relating to the number of items of data in each divided segment.

A reagent strip and a reagent analyzer for reading the reagent strip is described. The reagent strip includes a substrate, at least one reagent pad positioned on the substrate, and a photo luminescent phosphor spot positioned at a fixed location on the substrate. The photo luminescent phosphor spot is formulated to exhibit a predetermined addressable attribute.

An operator can perform exchange work of a reagent container without including a mechanism for reagent exchange and interrupting an analysis operation.

An automatic analyzer includes: an analysis unit including a plurality of operation units for performing analysis of a specimen; and a control unit for controlling the analysis unit. The control unit allows the analysis unit to set to at least (a) an analysis operation mode in which a first and a second operation unit are operated for the analysis of the specimen, (b) a partial operation mode in which only the first operation unit is continuously operated after the analysis of the specimen is completed in the analysis operation mode, and (c) a reagent exchange mode in which consumables containing a reagent are exchangeable in the analysis unit. The control unit allows the analysis unit to shift from the partial operation mode to the reagent exchange mode.

As a standard solution for evaluating a scattered light measuring optical system mounted on an automated analyzer, a standard solution containing an insoluble carrier at a concentration, at which transmittance is in a range of 10% to 50%, is used, and a light quantity of a light source is adjusted such that a scattered light detector outputs a predetermined value.

The method presented here is used to determine the volume dispensed by any liquid handling device (automated or manual) . A reference curve is first generated by spectroscopically reading a fixed-volume set of known, variable-concentration derivatives of a single dye. During testing the liquid handling device dispenses a yet undetermined volume of known-concentration dye into a known volume of diluent which results in a new dye concentration (resultant concentration). The absorbance of the resultant concentration is then compared to the absorbance vs concentration relationship of the earlier generated reference curve to determine the volume of dye (hence volume) dispensed by the liquid handling device. This method is an alternative to the dual dye and gravimetric volume verification methodologies. It considers and corrects for the uncertainties found in a traditional single dye approach as stated in the IWA-15 ISO standard. The system and method is distributed in bundled kits including but not limited to standardized labware, a calibrated reference pipette, a proprietary Validation Reference Plate (VRP) which automates reference curve generation, a spectrophotometer calibration plate for NIST Traceability, an environmental monitor, reference reagents, test reagents, an apparatus for quality assurance and control during manufacturing, and proprietary software for data analysis and reporting.

A method of conducting a biological assay, comprises obtaining data corelative to a temperature of a reagent, mixing the reagent with a sample to provide a mixture, receiving from the mixture a signal indicative of an amount of an analyte in the sample, and correcting the amount based on the obtained data and on a type of the reagent.