A device and method for increasing the concentration of an analyte in a fluid sample. The device may include: a housing defining a chamber therein for receiving a fluid sample, a membrane associated with the housing; and a pressure generator operatively connected to the housing to create a pressure gradient across the membrane. When the pressure generator is operated to create the pressure gradient, this causes at least a portion of the fluid sample to move across the membrane. As a result, the fluid sample is separated into a first portion of fluid and a second portion of fluid including said analyte on opposite sides of the membrane. This second portion of fluid by having the analyte present in an amount of fluid that is reduced as compared to the fluid sample prior to the application of pressure - is thus the resulting analyte-concentrated fluid sample.

Provided is a field-flow-fractionation apparatus that is configured to supply a carrier fluid to a waste fluid chamber through a fluid supply flow path at a flow rate higher than a set flow rate of a flow rate adjusting part at a timing between an end of analysis of a sample and a start of analysis of a subsequent sample, thereby forming a flow of the carrier fluid from the waste fluid chamber to the separation channel. Accordingly, the sample adhering to a separation membrane is separated from the separation membrane and is discharged from the outlet port.

Disclosed herein are rolled-membrane microfluidic diffusion devices and corresponding methods of manufacture. Also disclosed herein are three-dimensionally printed microfluidic devices and corresponding methods of manufacture. Optionally, the disclosed microfluidic devices can function as artificial lung devices.

Filtration apparatus for the assay of biological and biochemical reactants, for example, is provided and includes a substrate such as a plate having one or more wells open at each end, and a porous membrane positioned in each well forming a discrete filtering area. The filtration apparatus includes a seal that is in a compressible relationship with the face of the porous membrane, the surface of the compression element, and the well wall. Each well includes a compression element, such as an internal well insert or sleeve, which compresses the seal so that the seal contacts the membrane face, the surface of the compression element, and the well wall in a liquid-tight manner. The compression element may be configured so that it is fixed in the well such as by an interference fit with the well wall or by bonding to a surface of the substrate.

High-throughput microfluidic devices comprising one or more fluidic microchannels each with at least one flow-through 3D structure comprising a 3D electrode, or alternatively a 3D permselective structure, and optional secondary bead bed(s) are disclosed. Such devices can be used for counter-flow focusing of charged species via ion concentration polarization and in situ quantification of electrokinetically enriched charged species from an ionically conductive solution by both optical and electrical detection.

A porous membrane for use in an electroosmotic pump for pumping a fluid by electroosmotic transport, the porous membrane comprising: first and second opposite surfaces and a net fluid flow direction extending in the porous membrane between said opposite surfaces, wherein when a given amount of charge flows through the porous membrane from the first to the second opposite surface more electroosmotic transport of the fluid will occur than when the same amount of charge flows through the porous membrane from the second to the first, opposite surface.

A device for extracting and concentrating a target analyte including a sample channel that receives the sample, a separation channel, a waste channel, a first junction between the sample channel and the separation channel, and, a second junction between the separation channel and the waste channel. The first junction selectively transports a first group of analytes, including target analytes, from the sample channel to the separation channel in accordance with a size of a first free transport region of the first junction. The second junction selectively transports a second group of analytes from the separation channel to the waste channel in accordance with a size of a second free transport region of the second junction, the second group being a subset of the first group, so as to concentrate a number of the target analytes in the separation channel.

Embodiments of the present disclosure describe an isoporous polymer membrane comprising a polymeric film having a plurality of isopores, wherein the isoporous polymer membrane is characterized in that it has one or more of the following features: a porosity of about 20% or greater, a plurality of isopores arranged in an ordered array, wherein the plurality of isopores extend from a first membrane surface to a second membrane surface along an axis perpendicular to the first and second membrane surfaces, a membrane size of about 45 cm.sup.2 or greater, and a pore size of about 2 μm or less. Embodiments of the present disclosure also describe methods of fabricating the isoporous polymer membranes, applications using the isoporous polymer membranes, and the like.

In one embodiment, an optical spectroscopy probe includes an optical fiber having a distal tip and a microfluidic filtering chamber attached to the distal tip of the optical fiber, the chamber comprising a microfluidic membrane adapted to enable liquid to enter the chamber but prevent particles from entering the chamber.

Disclosed herein are rolled-membrane microfluidic diffusion devices and corresponding methods of manufacture. Also disclosed herein are three-dimensionally printed microfluidic devices and corresponding methods of manufacture. Optionally, the disclosed microfluidic devices can function as artificial lung devices.