Abstract: A lighting device for a vehicle has at least one headlamp having a plurality of lighting elements which are individually controllable. A method of controlling the lighting device includes detecting an activated state of the at least one headlamp; detecting a body to be protected from glare; determining a glare suppression angular range based on an extent and position of the body; and determining at least one transition angular range between the glare suppression angular range and a fully illuminated angular range. The light intensity of the glare suppression angular range is set below a specified limit The light intensity of the transition angular range depends on a distance of a beam angle of the individual lighting elements from the glare suppression angular range, wherein the light intensity increases with increasing distance.

Abstract: The present invention relates to a method of maturity classifying reticulocytes from a whole blood sample, comprising: staining the sample with a supravital agglutinating dyeing reagent or a fluorescent agglutinating dye; illuminating the stained sample with a light beam to detect reticulocytes; determining for each reticulocyte the parameters of (i) a fraction (?) of the reticulum area (Ar) to the whole cell area (Ac); and (ii) a fraction (?) of the perimeter of the reticulum (Ur) to the reticulum area (Ar); and maturity classifying a reticulocyte into 1 of 4 major maturity classes according to the values determined for ? and ?.

Abstract: An automatic analyzer for analyzing a medical probe includes an analysis cell for the probe, a piezo element, and an analysis device. The piezo element can be operated by applying a voltage and a frequency, and in the process an acoustic wave field is generated. A probe located in the analysis cell is located in the acoustic wave field when the piezo element is being operated.

Abstract: The invention relates to an in-vitro method for determining a cell type of a white blood cell in a biological sample without labeling, wherein a microscopy apparatus images the cell and physical parameters of the cell are ascertained from the image of the cell by means of an automated image analysis, wherein the cell type of the white blood cell is determined on the basis of the physical parameters and on the basis of principal component analysis parameters (PCA parameters), wherein the principal component analysis parameters comprise linear combinations of at least some of the physical parameters.

Abstract: The present invention relates to a method of detecting a possible infection of malaria in a patient using a digital optical microscope.

Abstract: The invention relates to an analyzer for analyzing a medical sample. The analyzer comprises an optical microscope for imaging a light field in an object region in order to image the sample. The microscope comprises a light source for illuminating the sample, an objective comprising a converging lens for concentrating and focusing light beams coming from the illuminated sample, and a digital recording device for recording the light beams. A light-field camera for capturing the light field from the object region, which light field is imaged in the microscope, is provided on the microscope.

Abstract: A computer-implemented method for analyzing digital holographic microscopy (DHM) data for hematology applications includes receiving a DHM image acquired using a digital holographic microscopy system. The DHM image comprises depictions of one or more cell objects and background. A reference image is generated based on the DHM image. This reference image may then be used to reconstruct a fringe pattern in the DHM image into an optical depth map.

Abstract: The invention relates to a device for examining particles in a liquid to be examined, comprising a flow passage through which the liquid to be examined is moved. The flow passage has at least one inlet through which at least one sheath fluid flows into the flow passage such that the at least one sheath fluid forms at least one sheath flow in the flow passage. The device further comprises a wave generating device for piezoacoustically generating sound waves which propagate through the flow passage transversely to the flow direction of the liquid to be examined and form wave nodes on a monitoring plane such that particles to be examined of the liquid to be examined are moved onto the monitoring plane and accumulate thereon on the basis of the pressure effect of the sound waves in the transverse direction.

Abstract: The present invention relates to an improved method for marker-free detection of a cell type of at least one cell in a medium using microfluidics and digital holographic microscopy, as well as a device, particular for carrying out the method.

Abstract: The present invention relates to a method of detecting a possible infection of malaria in a patient using a digital optical microscope

Abstract: A technique is presented for aligning, in a desired region within a flow chamber of a flow cell, a non-spherical biological entity carried in a sample. The flow chamber has a rectangular cross-section. A bottom flow input module, a top flow input module and a sample input module provide a viscoelastic first fluid, a second viscoelastic fluid, and the sample, respectively, to the flow chamber. The first and the second viscoelastic fluids laminarly flow along a bottom and a top wall of the flow chamber and the sample laminarly flows sandwiched between them. By controlling rate of flow of the first and/or the second viscoelastic fluids the sample flow, and thus the non-spherical biological entity, is focused in the desired region. A gradient of sheer within the sample flow set up due to the first and second viscoelastic fluids orients the non-spherical biological entity in the desired region.

Abstract: The invention relates to a cartridge (1) for a magnetic flow cytometer, mainly extending in a x-y-plane, with an inlet (2) for injecting a sample (15) into the cartridge (1), a blister (3) for a buffer solution (21) with magnetic markers to mark pregiven particles (16, 16?) of the sample (15), an outlet, and a fluid channel (9), the fluid channel (9) comprising a first part that connects the inlet (2) with the blister (3) and a second part that connects the first part with the outlet, wherein the second part of the fluid channel (9) comprises an enrichment zone (5) with mechanical guiding structures to focus marked particles (16, 16?) of the sample (15) in a predetermined subsection of the fluid channel (9) and a measuring zone (6) between the enrichment zone (5) and the outlet, the measuring zone (6) comprising a magnetic field sensor (14) in the predetermined subsection of the fluid channel (9) in order to provide simplified and accelerated means for measuring particles, in particular concentrations of part

Abstract: The present invention relates to an improved method for marker-free detection of a cell type of at least one cell in a medium using microfluidics and digital holographic microscopy, as well as a device, particular for carrying out the method.

Abstract: A technique is presented for aligning, in a desired region within a flow chamber of a flow cell, a non-spherical biological entity carried in a sample. The flow chamber has a rectangular cross-section. A bottom flow input module, a top flow input module and a sample input module provide a viscoelastic first fluid, a second viscoelastic fluid, and the sample, respectively, to the flow chamber. The first and the second viscoelastic fluids laminarly flow along a bottom and a top wall of the flow chamber and the sample laminarly flows sandwiched between them. By controlling rate of flow of the first and/or the second viscoelastic fluids the sample flow, and thus the non-spherical biological entity, is focused in the desired region. A gradient of sheer within the sample flow set up due to the first and second viscoelastic fluids orients the non-spherical biological entity in the desired region.

Abstract: The invention relates to a device for examining particles in a liquid to be examined, comprising a flow passage through which the liquid to be examined is moved. The flow passage has at least one inlet through which at least one sheath fluid flows into the flow passage such that the at least one sheath fluid forms at least one sheath flow in the flow passage. The device further comprises a wave generating device for piezoacoustically generating sound waves which propagate through the flow passage transversely to the flow direction of the liquid to be examined and form wave nodes on a monitoring plane such that particles to be examined of the liquid to be examined are moved onto the monitoring plane and accumulate thereon on the basis of the pressure effect of the sound waves in the transversal direction.

Abstract: A computer-implemented method for analyzing digital holographic microscopy (DHM) data for hematology applications includes receiving a DHM image acquired using a digital holographic microscopy system. The DHM image comprises depictions of one or more cell objects and background. A reference image is generated based on the DHM image. This reference image may then be used to reconstruct a fringe pattern in the DHM image into an optical depth map.

Abstract: The invention relates to a cartridge (1) for a magnetic flow cytometer, mainly extending in a x-y-plane, with an inlet (2) for injecting a sample (15) into the cartridge (1), a blister (3) for a buffer solution (21) with magnetic markers to mark pregiven particles (16, 16?) of the sample (15), an outlet, and a fluid channel (9), the fluid channel (9) comprising a first part that connects the inlet (2) with the blister (3) and a second part that connects the first part with the outlet, wherein the second part of the fluid channel (9) comprises an enrichment zone (5) with mechanical guiding structures to focus marked particles (16, 16?) of the sample (15) in a predetermined subsection of the fluid channel (9) and a measuring zone (6) between the enrichment zone (5) and the outlet, the measuring zone (6) comprising a magnetic field sensor (14) in the predetermined subsection of the fluid channel (9) in order to provide simplified and accelerated means for measuring particles, in particular concentrations of part

Abstract: An arrangement for modifying the local intensity of x-ray radiation includes an x-ray filter with a plurality of absorption chambers, which may be filled by a ferrofluid. The absorption chambers are stacked in the x-ray beam direction. The x-ray filter includes a plurality of storage containers in which the ferrofluid may be stored. Each of the absorption chambers is connected to a respective one of the storage containers. The absorption of the x-ray radiation is achieved as a result of individual absorption chambers being filled with the ferrofluid. By filling a different number of absorption chambers, the local intensity of the x-ray radiation may be modified easily, precisely and quickly.

Abstract: For flow cytometric measurement, a channel includes a magnetic sensor and is disposed downstream of a chamber. The chamber and the channel form a closed system, wherein an axis of the channel extends along a flow direction of the channel. A closed system is present if the chamber merges directly into the channel. A magnet, more particularly a permanent magnet, and a deflection device, are both arranged at a predefined side of the channel. Here, the deflection device has at least one segment. Each segment is arranged in a concentration region of the channel. Each segment has a guide for guiding cells toward the axis. The deflection device thus enables an enrichment of magnetically marked cells, which are pulled to the channel side by the magnet in the respective concentration region, on the axis and guidance of these cells along the axis to the magnetic sensor.

Abstract: The embodiments relate to an arrangement for quantifying cells of a cell suspension and enriching marked cells. The arrangement includes a fluid channel for routing the cell suspension with a first cross-section and a magnetic sensor on the fluid channel for counting magnetically marked cells in the cell suspension. The fluid channel has an enrichment region with a second cross-section which is larger than the first cross-section, a magnet being arranged on at least one side of the enrichment region.