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.

A biological fluid separation device adapted to receive a biological fluid sample having a first portion and a second portion is disclosed. The device includes a housing having a first chamber having a first chamber inlet for receiving the biological fluid sample therein and a first chamber outlet. The housing has a second chamber having a second chamber inlet and a second chamber outlet, and a separation member separating at least a portion of the first chamber outlet and the second chamber. The separation member is adapted to restrain the first portion of the biological fluid sample within the first chamber and to allow at least a portion of the second portion of the biological fluid sample to pass into the second chamber. An actuator, such as a vacuum source, draws the biological fluid sample into the first chamber and the second portion into the second chamber.

A membrane including a polymer substrate having pore channels and a metal-organic framework disposed on the polymer substrate. Methods of producing the membrane are described. Methods of separating gases using the membrane are also provided.

A biological fluid separation device adapted to receive a biological fluid sample having a first portion and a second portion is disclosed. The device includes a housing having a first chamber having a first chamber inlet for receiving the biological fluid sample therein and a first chamber outlet. The housing has a second chamber having a second chamber inlet and a second chamber outlet, and a separation member separating at least a portion of the first chamber outlet and the second chamber. The separation member is adapted to restrain the first portion of the biological fluid sample within the first chamber and to allow at least a portion of the second portion of the biological fluid sample to pass into the second chamber. An actuator, such as a vacuum source, draws the biological fluid sample into the first chamber and the second portion into the second chamber.

A filtration filter used for filtering a liquid chemical for lithography, provided with a polyimide resin porous membrane; a filtration method including allowing a liquid chemical for lithography to pass through the filtration filter; and a production method of a purified liquid chemical product for lithography, including filtering a liquid chemical for lithography by the filtration method.

A membrane for fluid transfer includes a base membrane and a pattern, that covers a working area of a surface thereof, formed of a compatible material. The pattern has periodicity and/or amplitude that do not exceed 1 micrometer. A method of filtering a component from a solution includes passing the solution comprising the component through a membrane that includes a base membrane. The base membrane and a pattern that covers a working area of a surface thereof are formed of materials compatible with the solution. The pattern has periodicity and/or amplitude that do not exceed 1 micrometer, and reduces mass transfer of surface-accumulative soluble and/or suspended species and particulates from the solution to the membrane while the solution is passed through the membrane. A method of producing a membrane for fluid transfer includes forming a nanoscale pattern over a working area of a polymer membrane.

A system for manufacturing a membrane filter is provided. The system includes a radiation source operative to emit radiation that contacts discrete portions of a filter substrate so as to facilitate the formation of openings within the filter substrate, and a collimator disposed between the filter substrate and the radiation source and operative to restrict some of the radiation from contacting the filter substrate.

Disclosed is a method for the production of a porous polymer membrane suitable for liquid filtration or analyte capture, comprising the steps of: providing a flowable composition (100) on a substrate (220) the composition including at least: photo-activatable monomer molecules, photo activation initiator molecules and photo-activation quencher molecules; providing one or more pulses (L) of laser light at at least one focal point in the composition of sufficient energy to locally polymerise the composition; moving the or each focal point relative to the previously polymerised composition in a continuous or stepwise predetermined manner to a multiplicity of further positions; and repeating the pulse(s) at those further positions such that a three dimensional matrix of the composition is polymerised leaving unpolymerized areas of a size equivalent to conventional polymer membrane pores.

Described are various embodiments of a method for fabricating a polymer membrane having open through holes, and membranes so produced. In some embodiments, a curable polymeric resin is introduced within a micro post structure wherein a material of the micro posts is soluble in a solvent and wherein the curable polymeric resin is insoluble in this solvent such that the structure can be at least partially dissolved to release the membrane once cured.

A method comprises forming etching islands on a substrate and exposing the substrate with etching islands to a solution that reacts with the etching islands to form a filter passage of interconnected pores in the substrate. The filter passage has an inlet into the substrate and an outlet from the substrate.