A device for agitating and collecting biological liquid samples comprises an agitator of racks of tubes, a sampling apparatus capable of collecting a biological liquid sample in a tube, and a changer capable of gripping a tube on a rack received in the agitator and moving it to the sampling apparatus. The agitator is capable of agitating at least three racks simultaneously, and the device also comprises a scheduler capable of determining destination data for a tube and destination data for the rack which receives this tube, and of determining for each tube a final location based on the destination data of the tube and the destination data of the racks received in the device, which final location designates a rack, received on the agitator and a position on this rack and can be different from the location of the tube when the rack that received it has been introduced into the device, and arranged to control the changer in order to grip a tube, present it to the sampling apparatus and replace it after sampling at the final location.

A filtering and ventilating mechanism is driven by motors. The filtering mechanism rotates and presses downwards so its pressing surface is against a sample container. A ventilation needle is inserted into the sample container for ventilation. A mixing mechanism is arranged below the filtering mechanism and is driven by a mixing motor. The sample container is accommodated in a seat and is driven by the mixing motor. A test tube carrying mechanism is arranged below the mixing mechanism, and has an accommodating hole for a test tube. A jacking mechanism is arranged below the mixing mechanism, and is driven by a jacking motor. When the jacking mechanism moves upwards, a jacking platform is pressed against the bottom of the test tube, so that the test tube is butted against the bottom of the sample container, and a sample preparation in the sample container is dripped into the test tube.

Methods and apparatus to mitigate bubble formation in a liquid are disclosed. An example apparatus disclosed herein includes a bottom wall, a first baffle cantilevered from the bottom wall, and a second baffle cantilevered from the bottom wall. The first baffle is spaced apart from the second baffle, and the first baffle and the second baffle are positioned radially relative to an axis of rotation of the apparatus.

A rotating device includes a carrier, a rotating plate, and a driving unit. The rotating plate rotatably connected with a pivot portion of the carrier contains a test liquid. The rotating plate or the driving unit has a stopping portion. When the driving unit drives the rotating plate to rotate so the stopping portion moves to a first position and interferes with the carrier, the driving unit applies driving force to the pivot portion of the carrier along a first rotation direction through the rotating plate. When the carrier rotates along the first rotation direction and the driving unit applies driving force to the rotating plate along a second rotation direction opposite to the first rotation direction, the rotating plate rotates relative to the carrier, the stopping portion moves to a second position and interferes with the carrier, and the driving unit applies driving force to the pivot portion of the carrier along the second rotation direction through the rotating plate.

A filtering and ventilating mechanism is driven by motors. The filtering mechanism rotates and presses downwards so its pressing surface is against a sample container. A ventilation needle is inserted into the sample container for ventilation. A mixing mechanism is arranged below the filtering mechanism and is driven by a mixing motor. The sample container is accommodated in a seat and is driven by the mixing motor. A test tube carrying mechanism is arranged below the mixing mechanism, and has an accommodating hole for a test tube. A jacking mechanism is arranged below the mixing mechanism, and is driven by a jacking motor. When the jacking mechanism moves upwards, a jacking platform is pressed against the bottom of the test tube, so that the test tube is butted against the bottom of the sample container, and a sample preparation in the sample container is dripped into the test tube.

A clinical instrument analyzer system for automated analysis of patient samples with a system for suspending particles or methods for the separation of particles, such as magnetic particles, is described herein. The system for suspending particles comprises a reagent cartridge comprising a reagent holder for holding a plurality of tubes. The plurality of tubes comprise a mixing tube for holding particles, rotatably mounted in the holder and a motor operatively connectable to a slot longitudinally positioned on the lower section of the mixing tube. The particles in the mixing tube are suspended when the mixing tube rotates in accordance with the embodiments of the invention. The analyzer can be used to analyze bodily fluid samples, such as blood, plasma, serum, urine or cerebrospinal fluid.

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.

The disclosure provides an apparatus for storing platelet-rich plasma (PRP). The apparatus is configured to reversibly receive a platelet-rich plasma (PRP) container. The apparatus comprises a platform defining at least one recess configured to receive the PRP container therein; and an agitator configured to move the platform, and thereby agitate PRP stored in the PRP container. The agitator is configured to move the platform in a circular motion at a frequency of between 10 and 10,000 revolutions per minute (RPM).

The disclosure provides an apparatus for storing platelet-rich plasma (PRP). The apparatus is configured to reversibly receive a platelet-rich plasma (PRP) container. The apparatus comprises a platform defining at least one recess configured to receive the PRP container therein; and an agitator configured to move the platform, and thereby agitate PRP stored in the PRP container. The agitator is configured to move the platform in a circular motion at a frequency of between 10 and 10,000 revolutions per minute (RPM).