A reaction processing apparatus includes: a reaction processing vessel; a temperature control system; and a liquid feeding system. The liquid feeding system includes: a pump having a discharge port; a first air channel; a second air channel; a first three-way valve capable of being switched between a state in which a first air communication port communicates with the discharge port and a state in which the first air communication port is opened to the atmospheric pressure; a second three-way valve capable of being switched between a state in which a second air communication port communicates with the discharge port and a state in which the second air communication port is opened to the atmospheric pressure; and a CPU that controls these components.

The present technology provides for a microfluidic substrate configured to carry out PCR on a number of polynucleotide-containing samples in parallel. The substrate can be a single-layer substrate in a microfluidic cartridge. Also provided are a method of making a microfluidic cartridge comprising such a substrate. Still further disclosed are a microfluidic valve suitable for use in isolating a PCR chamber in a microfluidic substrate, and a method of making such a valve.

A test system for analyzing a sample of a bodily fluid is provided and comprises: at least one test strip comprising at least one capillary channel comprising an inlet opening configured to receive the sample; a vent opening configured to provide an air vent to the capillary channel; and at least one zone consisting of a detection zone and a reagent zone; at least one measuring device configured for interacting with the test strip, the measuring device comprising at least one sealing element for hermetically sealing the vent opening from an ambient atmosphere; and at least one suction device adapted to provide an underpressure to the vent opening; wherein the measuring device further comprises at least one valve or is connectable to the valve, wherein the valve is configured to vent the vent opening of the test strip when the measuring device interacts with the test strip.

A fluid handling device has fluidic structures having inlet and outlet chambers and a connecting duct fluidically connecting the two. In a first state, the inlet chamber is completely or partly filled with at least a liquid and partly filled with a compressible medium, and the outlet chamber is at least partly filled with the compressible medium. One of the inlet chamber and the outlet chamber has such a venting duct that a flow resistance/volume product of venting of the chamber for the compressible medium amounts to at least 6700 N.Math.s/m.sup.2, the other of the inlet chamber and of the outlet chamber being vented. An actuator for actuating the fluidic structures is to cause a pressure difference of at least 30 Pa between the compressible media within the inlet and outlet chambers, so as to thereby switch a valve device implemented into the connecting duct.

Microfluidic structures and methods for manipulating fluids, fluid components, and reactions are provided. In one aspect, such structures and methods can allow production of droplets of a precise volume, which can be stored/maintained at precise regions of the device. In another aspect, microfluidic structures and methods described herein are designed for containing and positioning components in an arrangement such that the components can be manipulated and then tracked even after manipulation. For example, cells may be constrained in an arrangement in microfluidic structures described herein to facilitate tracking during their growth and/or after they multiply.

Aiming to provide a method capable of reciprocatingly delivering various liquids without bringing air into a microchannel, a detection system and a detection apparatus for implementation of this method. In order to achieve at least one of the above aims, provided is a method of inserting a pipette tip into a liquid injection portion of a detection chip including: the microchannel; the liquid injection portion connected to one end of the microchannel; and a reservoir connected to the other end of the microchannel, injecting and aspirating the liquid by the pipette tip, and reciprocatingly delivering the liquid into the microchannel. At this time, the following steps are executed in this order, the steps including: inserting the pipette tip into the liquid injection portion up to a position at which an end of the pipette tip comes below a liquid level when the liquid is injected into the liquid injection portion; injecting the liquid from the pipette tip into the liquid injection portion; generating a negative pressure in the liquid injection portion to raise the level of the liquid in the liquid injection portion; and performing either aspiration of the liquid in the liquid injection portion by the pipette tip, or injection of the liquid into the liquid injection portion by the pipette tip and aspiration of the liquid inside the liquid injection portion.

A centripetal microfluidic platform comprised of a microfluidics disc and a reader for testing LAL-reactive substances in fluid samples is provided. The microfluidic disc may comprise at least two testing areas wherein each testing area includes a reservoir portion for receiving at least one fluid sample. The disc may comprise a distribution network portion in fluid communication with the reservoir portion. Each distribution network portion may comprise a distribution network of at least four (4) channels, wherein each channel has a metering portion and at least one analysis chamber portion. The analysis chamber portion may comprise a mixing chamber for mixing samples and reagents and an optical chamber portion that is compatible with an optical reader. The metering portion may be sized to meter an aliquot of the fluid sample for analysis in the analysis chamber portion. At least one analysis chamber portion has at least one reagent isolated therein. The centripetal microfluidic platform further includes a reader for testing fluid samples within a microfluidic disc comprising an enclosure, an optical bench, a centripetal disc drive, and a controller. A method for testing at least one fluid sample for LAL-reactive substances is also provided.

Some embodiments of a blood coagulation testing system include an analyzer console device and a single-use cartridge component configured to releasably install into the console device. In some embodiments, the blood coagulation testing system can operate as an automated thromboelastometry system that is particularly useful, for example, at a point-of-care site.

A disposable electrochemical test sensor designed to facilitate sampling of fluid samples. It has a fluid chamber having a novel extra wide sampling entrance, but no additional air escape vent. The chamber provides a reservoir from which a sample fluid can be drawn into the chamber through capillary action. The extra wide sampling entrance provided by the present invention can draw blood into the chamber through any part of the opening, thus it allows easy targeting the samples with small volume, picking up smeared samples and it is more tolerant to users who jam the tip of the sensor into users'finger.

A nucleic acid amplifier may include a sample preparation zone, a fluid ejector, an amplification zone and a capillary break between the amplification zone and the fluid ejector.