A filtering device is provided to an analyzing instrument to block the passage of oversized particles that may otherwise clog the aperture of a sample analyzing device. The filtering device can be arranged to be proximate to the mixing chamber. In certain examples, the filtering device is placed at or adjacent an output port of the mixing chamber.

A biologic sample preparation system that prepares samples for processing includes a frame defining a horizontal plane, a pipette assembly, a sample module and an extraction module. The pipette assembly includes a first pipette. The pipette assembly is movably mounted to the frame in a direction substantially perpendicular to the horizontal plane during operation. The sample module includes a sample plate and is movably mounted to the frame. The sample module is movable substantially parallel to the horizontal plane at least from a sample area spaced from the pipette assembly and a working area proximate the pipette assembly. The extraction module includes an extraction plate and is movably mounted to the frame. The extraction module is movable substantially parallel to the horizontal plane at least from an extraction staging area spaced from the pipette, assembly and the working area proximate the pipette assembly.

Contamination detection systems, kits, and techniques are described for testing surfaces for the presence of hazardous contaminants, while minimizing user exposure to these contaminants. Even trace amounts of contaminants can be detected. A collection kit provides a swab that is simple to use, easy to hold and grip, allows the user to swab large areas of a surface, and keeps the user's hands away from the surface being tested. The kit also provides open and closed fluid transfer mechanism to transfer the collected fluid to a detection device while minimizing user exposure to hazardous contaminants in the collected fluid. Contamination detection kits can rapidly collect and detect hazardous drugs, including trace amounts of antineoplastic agents, in healthcare settings at the site of contamination.

A reagent storage device of the present disclosure includes a shutter and a moving mechanism. The shutter is configured to open and close an opening in a reagent compartment for housing a reagent container, the reagent compartment being provided with the opening for insertion and removal of a probe used to extract a reagent from inside the reagent container housed in the reagent compartment. The moving mechanism is configured to move the shutter to an overlay position opposing the opening and separated from the opening before moving the shutter downward so as to close off the opening, and is also configured to move the shutter that is closing off the opening upward to open up the opening before withdrawing the shutter from the overlay position over the opening.

The present invention determines whether or not a mounted tip and a dispensing amount match with each other in order to prevent contamination in a dispensing device. The present invention is provided with a pipette mechanism 108, 109 that performs suction and discharge, a motor 102 that drives the pipette mechanism, and a pressure sensor 113 that detects a pressure of the pipette mechanism. A dispensing tip 110 is mounted to the pipette mechanism. A control computer 116 controls the motor 102, drives the pipette mechanism in a suction or discharge direction, and determines a type of the dispensing tip 110 on the basis of a difference in pressure waveform detected by the pressure sensor 113.

A sample measurement method of performing first measurement for a blood coagulation test and second measurement for a test different from the blood coagulation test includes: dispensing a sample for use in the first measurement into a first container from a sample container; dispensing the sample for use in the second measurement into a second container different from the first container from the sample container from which the sample for use in the first measurement has been dispensed; performing the first measurement based on the sample dispensed into the first container; and performing the second measurement based on the sample dispensed into the second container.

Apparatuses and methods for generating trace vapors are provided. The apparatus includes a controller and an oven. The controller includes: a processor, a memory storing at least one control program, a clean solution supply port constructed to output a clean solution, an analyte solution supply port constructed to output an analyte solution, a carrier gas inlet port constructed to receive a carrier gas, and a plurality of carrier gas supply controllers constructed to output the carrier gas. The oven includes a clean manifold, an analyte manifold, a clean solution nebulizer constructed to: receive the clean solution from the clean solution supply port, and the carrier gas from one of the plurality of carrier gas supply controllers, and output a clean solution vapor stream comprising the clean solution and the carrier gas to the clean manifold, an analyte solution nebulizer constructed to: receive the analyte solution from the analyte solution supply port and the carrier gas from another one of the plurality of carrier gas supply controllers, and output an analyte solution vapor stream comprising the analyte solution and the carrier gas to the analyte manifold, a pneumatic valve controllably connected to the processor and communicatively connected to the clean manifold and the analyte manifold, and an output supply port communicatively connected to the pneumatic valve. The controller is configured to operate the pneumatic valve to allow the clean vapor solution or the analyte vapor solution to enter the chamber and be provided to the output supply port.

Provided is an automatic analyzer which does not require a preparation operation of disposing of a reaction vessel on the apparatus in advance and is capable of efficiently performing shifting to an analysis operation.

In a reaction promotion unit 108, a holding position located at a reaction vessel disposal position 202 during a first operation cycle is moved to a reaction vessel setting position 201 after an n (n: integer) operation cycle, and from a first operation cycle to an n-th operation cycle, an expendable item transport unit 112 performs an operation of disposing of a reaction vessel from a disposal position without performing an operation of setting the reaction vessel at a setting position in each operation cycle, and performs an operation of setting the reaction vessel at the setting position and an operation of disposing of the reaction vessel from the disposal position in each operation cycle after an (n+1)-th operation cycle.

Methods, systems, and devices for non-invasive measurement of cell cultures are described that provide for remote monitoring of cell status. The system includes a cell culture vessel, at least one monitoring layer, at least one measurement device, and a communication component. The cell culture vessel may include at least one cell culture chamber configured for cell growth and for closed-system operation. The monitoring layer is external to the at least one cell culture chamber. In some cases, the communication component is configured to transmit data from the monitoring layer to a remote location.

The present invention involves a fill needle system for aseptically dispensing a pharmaceutical fluid in an aseptic chamber comprises a fill needle tubing in fluid communication with a pharmaceutical fluid source via flexible tubing and extending through a fill needle hub; a fill needle dispensing tip disposed at a dispensing end of the fill needle tubing; a fill needle sheath shaped and arranged to removably mate with and seal aseptically to the fill needle hub to form an aseptically sealed volume enclosing the dispensing tip; and a fluid pressure pulse induction system disposed and configured to compress the flexible tubing in order to dislodge droplets of pharmaceutical fluid retained on the dispensing tip after halting dispensing of the pharmaceutical fluid. An associated method of dispensing pharmaceutical fluid comprises operating the fluid pressure pulse induction system to dislodge the droplets. The system may comprise a controller for automatically controlling the dispensing and droplet dislodging.