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.

A method for manufacturing a porous device (10) is described. The method comprises creating (340) a carbon nanomembrane (40) on a top surface (22) of a base material (20) having latent pores (23) and etching (360) the latent pores (23) in the base material (20) to form open pores (24). The porous device (10) can be used as a filtration device.

One aspect of the present disclosure provides a production method for a porous membrane including pores, and concave portions having an average opening diameter greater than an average pore diameter of the pores on at least one of a pair of main surfaces, the method including a step of forming the concave portion on a surface to be the main surface.

The present disclosure relates to a transport mechanism apparatus for transporting at least one of a gas or a fluid. The transport mechanism may have an inlet, an outlet and a triply periodic minimal surface (TPMS) structure. The TPMS structure is formed in a layer-by-layer three dimensional (3D) printing operation to include cells propagating in three dimensions, where the cells include wall portions having openings, and where the cells form a plurality of flow paths throughout the transport mechanism from the inlet to the outlet, and where the cells form the inlet and the outlet.

Track-etched membranes for filtration are provided. Filtration methods utilizing such membranes and cell culture methods are also provided.

Methods and apparatus provide filtration for concentrating analytes, such as bacteria or exosomes, of a biological sample, such as blood or urine. The technology may employ membrane devices that implement one or more tangential flow filtration processes such as in stages. An example membrane device may typically include a membrane having sides and ends. The membrane may selectively permit constituent(s) of the sample to pass through while retaining other constituents at one side. An input chamber of the device may include an inlet near one end and an outlet near the other end, and that may permit a tangential flow of the sample along the first side surface, and a trans-membrane passing of constituent(s). An output chamber of the device may be configured at the second side surface to receive the passing constituents. Such devices may be provided in a kit to facilitate targeting of a desired biological analyte concentration.

Filtration membrane with improved mechanical stability and increased resistance to pressure is provided. The filtration membrane is useful for in vivo implantable filtration devices, such as, an artificial kidney. In vivo implantable filtration devices are also provided.

Systems and methods described herein may produce a modified substrate. A process for producing a modified substrate may include providing a substrate that is 5 microns or less in thickness, ion tracking the substrate, and etching the tracked substrate with an etchant to produce a plurality of pores in the substrate. In some implementations, the substrate may be a polymer. In some implementations, the ion tracking may include controlling a flux of ions passing through the substrate to achieve a desired pore density. In some implementations, the track-etching of the substrate may create a 10% or more porosity in the substrate. In some implementations, the process may further include using the track-etched substrate as a support substrate for at least one of a single-layer graphene film, multi-layer graphene film, stack of graphene films, nanostructure of graphene flakes, or nanostructure of graphene platelets.

The invention relates to a gas in/outlet-adapter system for a container/rack assembly for a diagnostic robot comprising: —a receptacle (15) comprising a gas-inlet wherein the receptacle (15) is attached to a container (12), —a nozzle (16) comprising a gas-outlet wherein the nozzle (16) is attached to a rack to supply the container (12) via the receptacle (15) with a gas at a defined pressure level, wherein the receptacle (12) —provides one opening (24) —which provides for a fluidic contact to the interior of the container (12) —and a second opening (25) —which provides for a gas leak-proof connection to the nozzle (16) on the rack when the receptacle (15) is placed over the nozzle (16), and wherein the nozzle (16) —provides one opening (26) —which provides for a fluidic contact to a tubing system of the rack—and a second opening (27) —which provides for a fluidic contact to the nozzle (16) when the receptacle (15) is placed to cover the nozzle (15).

A microfilter, a manufacturing method thereof, and a microfiltration unit for holding the microfilter are provided. The microfilter has: a non-epoxy based microfilm; and a plurality of microholes provided on the surface of the non-epoxy based microfilm and penetrating therethrough via UV laser ablation, wherein the surface of the non-epoxy based microfilm is patterned into predetermined sections for locating isolated targets and quick enumeration.