An isolation device for isolation of target particles from a plurality of liquid samples includes a plurality of isolation chips and a vacuum system. Each of the plurality of isolation chips includes a sample reservoir, and a first outlet and a second outlet disposed at opposite sides of the sample reservoir. The vacuum system includes a first vacuum pump connected to the first outlet of each of the plurality of isolation chips and a second vacuum pump connected to the second outlet of each of the plurality of isolation chips. The first vacuum pump generates a negative pressure in each of the plurality of isolation chips through a corresponding first outlet. The second vacuum pump generates a negative pressure in each of the plurality of isolation chips through a corresponding second outlet. The target particles are isolated from each of the plurality of liquid samples in a corresponding sample reservoir.

The invention relates to a dialysis cell for sample preparation for a chemical analysis method, in particular for ion chromatography. The dialysis cell comprises a donor channel and an acceptor channel extending parallel thereto. The donor channel and the acceptor channel are separated from each other by a selectively permeable dialysis membrane. In particular, an analyte that is dissolved in a donor solution in the donor channel can enter through the dialysis membrane into the acceptor solution in the acceptor channel. The acceptor channel has at least in some sections a volume that is smaller than the volume of the donor channel extending parallel thereto. Acceptor and donor channels are formed from half-cells, between which the dialysis membrane is arranged, wherein the donor channel and the acceptor channel are designed in each case as a recess in a contact surface of one of the half-cells with the dialysis membrane.

A microfluidic detection system for micrometer-sized entities, such as biological cells, includes a detector component incorporating a plate with a plurality of opening, the plate separating two chambers, one in communication with a fluid source containing target entities bound to magnetic beads. The openings are sized to always permit passage of the magnetic beads therethrough into a lower one of the chambers and are further sized to always prevent passage of the target entities from the upper one of the chambers. The detector component further includes a magnet positioned to pull unbound magnetic beads through the openings and to capture target entities bound to magnetic beads on the surface of the plate. In a further feature, the microfluidic detection system is configured to pass target molecules through the plate to be bound to a functionalized surface of the lower chamber.

A device and method for isolating extracellular vesicles from biofluids is disclosed. A nanoporous silicon nitride membrane is provided with a tangential flow of biofluid. A pressure gradient through the nanoporous silicon nitride membrane facilitates capture of extracellular vesicles from the tangential flow vector of biofluid. Reversal of the pressure gradient results in the release of the extracellular vesicles for subsequent collection.

The disclosure provides a method for evaluation of removal of nitrogen-containing organic matter from the wastewater. The method includes: 1) pretreating a wastewater sample from a wastewater treatment plant; enriching nitrogen-containing organic matter in the wastewater sample with a solid-phase extraction cartridge; separating the nitrogen-containing organic matter from a substrate and disruptors of the wastewater sample, and collecting the nitrogen-containing organic matter; 2) detecting and analyzing the nitrogen-containing organic matter collected in 1) with a Fourier-transform ion cyclotron resonance mass spectrometer, thereby obtaining mass spectra of the nitrogen-containing organic matter; 3) preprocessing peak data of the mass spectra of the nitrogen-containing organic matter in each wastewater sample; setting the nitrogen-containing organic matter corresponding to the peak data as a global variable; arranging wastewater samples into cross-sectional data according to wastewater treatment processes; creating an assessment matrix for evaluating removal of the nitrogen-containing organic matter.

A method for purifying protein substrates for Real-Time Quaking Induced Conversion (“RT-QuIC”) is provided that can efficiently yield purified protein substrates desirable for RT-QuIC testing. By modifying certain parameters of the protein solubilization, the purification receptacle, the dialysis treatment, and the storage conditions, the purification and production of prion protein amplification substrate useful for RT-QuIC testing can be optimized.

A sampling device including an intake pump coupled with a volume controller to provide a known volume of samples such as liquid collected through a specialized hollow membrane filter. Once the known volume of sample is filtered the intake pump is turned off, an air pump turns on and removes residual or excess sample. The membrane filter is then preserved for extraction of DNA/RNA.

A system for separating and concentrating ionic compounds in a sample is provided herein. In some embodiments, a system includes at least one sample separation device, a flexible holder having a plurality of slots, wherein each slot is configured to have a sample separation device inserted therein, wherein the at least one sample separation device is inserted into a slot of the flexible holder; and an electrode for applying a voltage to the device, wherein the at least one sample separation device comprises a separation portion, a first storage portion, and a second storage portion, wherein the first and second storage portions are positioned on opposing sides of the separation portion, wherein the separation portion is folded at a predetermined interval to form two or more discrete base units.

A microfluidic detection system for micrometer-sized entities, such as biological cells, includes a detector component incorporating a plate with a plurality of opening, the plate separating two chambers, one in communication with a fluid source containing target cells bound to magnetic beads. The openings are sized to always permit passage of the magnetic beads therethrough into a lower one of the chambers and are further sized to always prevent passage of the target cells from the upper one of the chambers. The detector component further includes a magnet positioned to pull unbound magnetic beads through the openings and to capture target cells bound to magnetic beads on the surface of the plate. The microfluidic detection system includes a pump flowing the fluid through the detector component at high flow rates of milliliters per minute for high throughput detection of target cells.

The invention provides a gas detection system and a method with eliminating influence of ambient temperature and humidity change, the gas detection system comprises a bare sensor, a reference sensor and a calculation module; the bare sensor is used to detect a target gas in an ambient gas to obtain a first feedback signal; the reference sensor is used to selectively isolate the target gas in the ambient gas to produce a zero gas and to detect the zero gas to obtain a second feedback signal, the calculation module is used to calculate a difference between the first feedback signal and the second feedback signal to obtain a third feedback signal, and to obtain a target gas concentration by calculating the third feedback signal according to a calibration formula. The invention improves the measurement accuracy to the target gas concentration, which are efficient and reliable and have good technical effects.