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.

The present disclosure provides a porous membrane made of pentablock copolymer. The porous membrane includes an ABCBA block copolymer and has a number of pores. The A block is immiscible with each of the B block and the C block, the B block has a glass transition temperature (T.sub.g) of 90 degrees Celsius or greater, and the C block has a T.sub.g of 25 degrees Celsius or less. The A block comprises a poly(alkylene oxide), a substituted epoxide, a polylactam, or a substituted carbonate; B block comprises a vinyl aromatic monomer or a polyalkylmethacrylate and C block comprises a polyacrylate, a polysiloxane or a polyisoprene. A method of making a porous membrane is also provided. The method includes forming a film or a hollow fiber from a solution including a solvent and solids containing an ABCBA block copolymer. The method further includes removing at least a portion of the solvent from the film or the hollow fiber and contacting the film or the hollow fiber with a nonsolvent.

A filtration cell (10) for a biological sample having an outer housing (12) defining a first chamber and an inner housing (14) defining a second chamber is disclosed. The inner housing is disposed within the first chamber and rotatable with respect to the outer housing and at least a portion of the inner housing includes a filtration membrane (52). Upon rotation of the inner housing, a first portion of the biological sample passes from the first chamber into the second chamber and a second portion of the biological sample is restrained in the first chamber. Alternatively, the filtration cell may also include a rotation element disposed in the inner housing. Upon rotation of the rotation element with respect to the inner housing, a first portion of the biological sample to passes from the second chamber into the first chamber and a second portion of the biological sample is restrained in the second chamber.

The present disclosure provides apparatus and methods for processing liquids or fluids. Such apparatus and methods are convenient and efficient for low-cost separation, filtration, capture, collection, and/or storage of biologics and related materials. Provided apparatus and methods are designed for point-of-care use and offer advantages for patients and medical practitioners, including advantages in diagnosis and long-term monitoring of conditions.

An apparatus for roll-to-roll nanomaterial dispersion papermaking includes a suction pressure for consolidating nanomaterials on a fluid permeable filter in one region of the filter and an opposite pressure region or regions for separating a mat of the consolidated nanomaterials and transferring the mat to a transfer roller. A transfer roller may have a suction pressure within the transfer roller to help transfer the mat from the filter to the transfer roller, for example. An inlet port distributes nanomaterials using row and zone inlets, for example.

An apparatus for roll-to-roll nanomaterial dispersion papermaking includes a suction pressure for consolidating nanomaterials on a fluid permeable filter in one region of the filter and an opposite pressure region or regions for separating a mat of the consolidated nanomaterials and transferring the mat to a transfer roller. A transfer roller may have a suction pressure within the transfer roller to help transfer the mat from the filter to the transfer roller, for example. An inlet port distributes nanomaterials using row and zone inlets, for example.

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 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 process for manufacturing an article, comprising the step of manufacturing the article via an additive fabrication process from a structural material, is notable in that the structural material comprises a polymer selected from the following group: (co)polycarbonates, polyesters, polyestercarbonates, polyformals, polyamides, polyethers, polyvinyl chloride, polymethyl (meth)acrylate, polystyrene or a combination of at least two thereof and an additive absorbing infrared radiation. The additive absorbing infrared radiation is selected for its chemical structure and its concentration in the structural material such that it reduces transmission by the structural material of light in the wavelength range between 600 nm and 1700 nm, determined on a sample 100 ?m thick, by ?2.5 percentage points relative to a structural material sample with a thickness of 100 ?m that does not contain the additive absorbing infrared radiation. During the additive fabrication process the structural material is exposed at least temporarily to infrared radiation in the wavelength range between 600 nm and 1700 nm. An article obtainable by a process as described above is notable for its production from a structural material which comprises a polymer selected from the following group: (co)polycarbonates, polyesters, polyestercarbonates, polyformals, polyamides, polyethers, polyvinyl chloride, polymethyl (meth)acrylate, polystyrene or a combination of at least two thereof and an additive absorbing infrared radiation, where the article, in the direction of its construction in the additive manufacturing process used to make it, has a tensile strength (ISO 527) which is >30% to . . . 100% of the tensile strength (ISO 527) of a specimen injection-moulded from the same structural material.

A novel or improved base film for impregnation, impregnated base film, product incorporating the impregnated base film, and/or related methods as shown, claimed or described herein.