Robert Boschgmbh

Martina Daub

Jochen Rupp

Michael Stumber

Christian Dorrer

Thomas Brettschneider

Peter Rothacher

Martin Stelzle

Nils Paust

Juergen Steigert

Manuela Schmidt

Lars Sodan

Sven Zinober

Felix Von Stetten

Daniel Czurratis

Michael Hortig

Guenter Roth

Holger Behrens

Massimo Kubon

Yvonne Beyl

Jan Weile

Arne Kloke

Susanne Muench

Meike Moschallski

Melanie Hoehl

A film bag for storing a fluid, in particular a reagent or an auxiliary agent for a biochemical analysis method, includes a film, a seam, and an irreversibly destructible predetermined breaking point. The film is impermeable to the fluid and constituents of the fluid. The seam is formed in a fluid-tight manner between a first sub-region of the film and a second sub-region of the film and forms the film into a fluid-tight bag for accommodating the fluid. The bag is configured to be arranged in a chamber of a device that provides a fluid for a biochemical evaluating unit. The predetermined breaking point is formed from the film and is fluid-tight when a fluid pressure in the film bag is below a limit. The predetermined breaking point is destroyed when the fluid pressure is above the limit.

Film bag for storing a fluid and device for providing a fluid

A device configured for lysing a sample includes a holding element configured to hold an energy-transmitting element such that the holding element lies around the held part of the energy-transmitting element and envelops the held part of the energy-transmitting element and/or that the holding element lies against the held part of the energy-transmitting element. The holding element is further configured to cause lysis with the energy-transmitting element when the holding element is immersed into the sample to be subjected to lysis or comes into contact with the sample to be subjected to lysis. A method includes inserting the energy-transmitting element into the holding element. A system configured for lysing a sample by way of ultrasound includes the device and the energy transmitting element.

Devices, method and system employable for lysing

A method for active hybridization in microarrays includes pumping an already prepared sample through a denaturing unit with a microarray and then through a reaction region which is spatially separate from the denaturing unit. The denatured reactive sample components are hybridized in the reaction region.

Method for active hybridization in microarrays with denaturing function

A mixing chamber includes a container for receiving a first and a second component; an obstacle structure, which is designed such that, under the effect of a centrifugal force or magnetic force acting on the mixing chamber, it moves through the first and second components in the container and mixes them with each other; and a connection piece, which is connected at one end to the container and at the other end to the obstacle structure.

Mixing chamber, cartridge, and method for mixing a first and a second component

A microneedle array applicator is configured to apply a microneedle array in cosmetic and medical applications. The microneedle array applicator has a holding apparatus configured to define detachable holding of a microneedle array comprising a planar substrate. The microneedle array applicator also has a drive mechanism for driving the microneedle array in a first direction perpendicular to the planar substrate and in a second direction parallel to the planar substrate. A method for applying a microneedle array includes the microneedle array applicator enabling safe breaking off of the microneedles, optionally laden with an active ingredient, in the skin.

Microneedle array applicator and method for applying a microneedle array

A cartridge is configured for insertion and centrifugation in a centrifuge. The cartridge includes a mixing chamber, which comprises a container that is configured for at least one first component and at least one second component and electromagnetic particles. The electromagnetic particles are movable by an electromagnetic force to mix the first and second components.

Cartridge, centrifuge and method for mixing a first and second component

A method is disclosed for concentrating sample constituents and for multiplying nucleic acids from a biological sample which are containing in the sample constituents. The nucleic acids are amplified on the same filter on which the sample constituents are also separated off.

Method for concentrating sample constituents and for multiplying nucleic acids from a biological sample which are contained in the sample constituents

A cartridge includes a first drum having a first chamber and a displacement device that is configured to rotate the first drum about a central axis to connect the first chamber to a second chamber in a conductive manner. The cartridge further includes an electric switch that is configured to be actuated by the displacement device between a closed switching state and an open switching state.

Cartridge, centrifuge and method

A microfluidic system comprises a cartridge that includes a first drum which has a first chamber and an adjustment device which is arranged so as to rotate the first drum about its mid-axis and is configured to connect the first chamber conductively to a second chamber. The microfluidic system further comprises a pressure device which acts upon at least one component with a pressure difference and is configured to transfer the component between the first chamber and second chamber.

Microfluidic system and method for operating such a system

A microsystem for fluidic applications includes a substrate with a reservoir, a first microchannel, connected to the reservoir, and a second microchannel, separated from the first microchannel by a fixed member. The microsystem furthermore has an elastic film on the substrate, which film has a joint to the substrate around the reservoir and seals the reservoir. Here, the joint has a permanent joining area and, on the fixed member, a fixed member joining area that can be broken open and adjoins the permanent joining area at both ends of the fixed member. Such a microsystem forms a processing chip with reagent receptacle.

Microsystem for fluidic applications, and production method and usage method for a microsystem for fluidic applications

A cartridge is configured for insertion and centrifugation in a centrifuge. The cartridge includes a first drum which has a first chamber, and a displacement device which is designed to rotate the first drum about a center axis thereof to selectively and conductively connect the first chamber to a second or a third chamber. In another embodiment, the cartridge includes a first drum which has a first chamber and a second chamber, and a displacement device which is designed to rotate the first drum about the center axis thereof to selectively and conductively connect the first chamber to a third chamber or the second chamber to the third chamber. The displacement device has an actuator which directly or indirectly moves the first drum about the center axis.

A microfluidic cell for the dielectrophoretic separation, accumulation, and/or lysis of polarizable bioparticles, including an interdigital electrode system composed of two electrode groups having interdigitated electrodes, and a micromixer having microchannels and microelevations. The interdigital electrode system and the micromixer are situated on the same side of the cell to improve the separation, accumulation, and/or lysis characteristics. Moreover, also described is a microfluidic system which includes such a microfluidic cell, and use thereof, and a method for separating, accumulating, and/or lysing polarizable bioparticles.

Microfluidic cell

A method for producing a multilayer system with at least two joining elements, these being produced in particular from plastic, is disclosed. The method includes applying a compensating means, for at least partially compensating for mechanical stresses, to a first joining element, applying a second joining element to the compensating means, for joining together the first and second joining elements, firstly connecting the first joining element to the compensating means and secondly connecting the second joining element to the compensating means. A corresponding multilayer system and a corresponding use is also disclosed.

Method for producing a multilayer system and corresponding multilayer system

A device and a method for optical parallel analysis of a sample arrangement. The device includes a system of sample areas provided on and/or in a front face of the carrier substrate for receiving a sample substance; a system of detector areas provided on and/or in a back face of the carrier substrate, each detector area being assigned to a corresponding sample area; and a system of optical devices, each optical system being assigned to a corresponding sample area and being designed in such a way that it deflects light beams, which the corresponding sample area in response to an optical excitation does not emit in the direction of a detector area assigned to it, in the direction of the detector area assigned to it and/or in the direction of a detector-free area on the back face of the carrier substrate.

Growing community of inventors

Weissach, Germany

Martina Daub