The invention relates to a method, to a device, and to a system for the automated determination of optical densities or of the change in optical densities of reaction mixtures in shaken reactors during shaking operation. Methods and devices currently used therefor are often unreliable, are susceptible to environmental and process factors, or require interruptions to the shaking operation that impair the process control. The problem addressed by the invention is that of specifying a method and a device for the automated determination of optical densities or of the change in optical densities of reaction mixtures in shaken reactors during shaking operation that operate reliably under various environmental and process conditions. This problem is solved by means of a new measurement method, wherein the reaction mixture distribution, which periodically fluctuates because of the shaking action, is used to record measurement points (20/21) of transmission/scattered-light measurements, which measurement points fluctuate periodically as a result of shaking. All measurement points (20/21) of a measurement operation are combined into a measurement series (34), from which the optical density and/or the change in the optical density, and other process parameters, can be determined with high reliability by means of suitable mathematical methods. The invention is suitable in particular for biotechnological, pharmaceutical, chemical, and biochemical screening and optimization and process-monitoring applications.

The invention relates to a method, to a device, and to a system for the automated determination of optical densities or of the change in optical densities of reaction mixtures in shaken reactors during shaking operation. Methods and devices currently used therefor are often unreliable, are susceptible to environmental and process factors, or require interruptions to the shaking operation that impair the process control. The problem addressed by the invention is that of specifying a method and a device for the automated determination of optical densities or of the change in optical densities of reaction mixtures in shaken reactors during shaking operation that operate reliably under various environmental and process conditions. This problem is solved by means of a new measurement method, wherein the reaction mixture distribution, which periodically fluctuates because of the shaking action, is used to record measurement points (20/21) of transmission/scattered-light measurements, which measurement points fluctuate periodically as a result of shaking. All measurement points (20/21) of a measurement operation are combined into a measurement series (34), from which the optical density and/or the change in the optical density, and other process parameters, can be determined with high reliability by means of suitable mathematical methods. The invention is suitable in particular for biotechnological, pharmaceutical, chemical, and biochemical screening and optimization and process-monitoring applications.

Disclosed are devices and methods for performing biological and chemical assays, such as immunoassays and nucleic acid assays, more particularly a homogeneous assay that does not use a wash step by using the aggregation and de-aggregation processes of microparticles or nanoparticles.

Systems and methods for analysis of a whole blood sample from an individual to determine the platelet function and coagulation status of the individual in a substantially automated and efficient matter. Also provided here are systems, reagent kits, and methods for concurrent assessment of platelet function and coagulation as they interact during hemostasis.

Systems and methods for analysis of a whole blood sample from an individual to determine the platelet function and coagulation status of the individual in a substantially automated and efficient matter. Also provided here are systems, reagent kits, and methods for concurrent assessment of platelet function and coagulation as they interact during hemostasis.

Machine learning analysis for classifying agglutination of fluid samples. A method includes scanning a unique scannable code printed on a test card, wherein the test card comprises a negative control fluid sample, a positive control fluid sample, and a test fluid sample. The method includes capturing an image of the test card and providing the image of the test card to a machine learning algorithm configured to assess agglutination of the test fluid sample based on the image. The method includes receiving from the machine learning algorithm one or more of a qualitative analysis or a quantitative analysis of the agglutination of the test fluid sample.

Method for detecting the presence or absence of a biological or chemical substance in a particular sample mixed with a suspension with functionalized magnetic particles, comprising: providing a light source and detector, providing a constant magnetic force perpendicular to the light's propagation direction by applying a constant magnetic field gradient, and with an absolute value which is higher than 0.1 T and measuring the change of the magnetic particle's suspension transparency versus time and comparing it with the time-variation in absence of the targeted biological or chemical substance. The method of the invention allows monitoring the transparency irrespective of the emitted wavelength and particle's optical properties.

An example system includes a chamber to hold a mixture that includes a whole blood sample from a patient, a light source to illuminate the mixture in the chamber, a detector to detect light from the light source transmitted through the mixture in the chamber, and one or more processing devices to determine, based on the light detected by the detector, a platelet aggregation value of the whole blood sample that is substantially independent of a hematocrit of the whole blood sample.

The disclosure directed to methods for measuring an analyte alone or in combination with total protein in biological samples. More particularly, the disclosure relates to methods for measuring an analyte and/or total protein using one or more colorimetric reagents alone or in combination with protein precipitation reagents.

The disclosure directed to methods for measuring an analyte alone or in combination with total protein in biological samples. More particularly, the disclosure relates to methods for measuring an analyte and/or total protein using one or more colorimetric reagents alone or in combination with protein precipitation reagents.