A system, method and device are disclosed for bio-processing a feed stream and providing a constant output by operating a continuous single-pass tangential-flow process. The single-pass process provides high conversion concentration while operating at relatively low feed flow rates, and the process can also be used to provide constant output diafiltration.

A technology that provides various modular biomimetic microfluidic modules emulating varieties of microvasculature in body. These microfluidic-base capillaries and lymphatic Technology modules are constructed as multilayered-microfluidic microchannels of various shapes, and aspect ratios using diverse biocompatible microfluidic polymers. Then, various semipermeable membranes are sandwiched in between these multilayered microfluidic microchannels. These membranes have different chemical, physical characteristics and MWCO values. Consequently, this design will produce much smaller dimension channels similar to human vasculature to achieve biomimetic properties like of human organs and tissues. By interchanging microfluidic-layers or the membranes various diverse modules are designed that act as building blocks for constructing various medical devices, various forms of dialysis devices including albumin and lipid dialysis, water purification, bioreactors, bio-artificial organ support systems. Connecting various modules in diverse combinations, permutations, in parallel and/or in series to ultimately design many unrelated medical devices such as dialysis, bioreactors and organ support devices.

A filter medium according to one embodiment of the present invention comprises: a first support having a plurality of pores; a nanofiber web comprising nanofibers disposed on upper and lower portions of the first support and forming a three-dimensional network structure, and a hydrophilic coating layer formed on at least a part of an outer surface of the nanofibers, wherein the hydrophilic coating layer is formed of a hydrophilic coating composition comprising a hydrophilic polymer compound having at least one functional group selected from a hydroxyl group and a carboxyl group and a crosslinking agent comprising at least one sulfone group; and a second support having a plurality of pores interposed between the first support and the nanofiber web.

A filter medium according to one embodiment of the present invention comprises: a first support having a plurality of pores; a nanofiber web comprising nanofibers disposed on upper and lower portions of the first support and forming a three-dimensional network structure, and a hydrophilic coating layer formed on at least a part of an outer surface of the nanofibers, wherein the hydrophilic coating layer is formed of a hydrophilic coating composition comprising a hydrophilic polymer compound having at least one functional group selected from a hydroxyl group and a carboxyl group and a crosslinking agent comprising at least one sulfone group; and a second support having a plurality of pores interposed between the first support and the nanofiber web.

An inline filter housing with a biodegradable, hydrophilic material that operates in conjunction with a field sampling apparatus to both concentrate field sampled environmental DNA particles from water samples and to automatically preserve the captured DNA via desiccation, thus avoiding filter membrane transfer steps, chemicals or cold storage preservation requirements. The hydrophilic filter housing is capable of rapidly preserving the field sampled environmental DNA captured on the filter membrane at ambient field temperatures.

A filtration module for filtering a process medium in a bioprocess including a process flow path for a process medium, a filter membrane coupled to the process flow path, and a sampling membrane coupled both to the process flow path and to a sampling flow path for extracting a sample from the process medium. The sampling flow path guides the extracted sample to a sampling outlet of the filtration module or to an analyzer integrated into the filtration module. A filtration assembly including the filtration module and an analyzer coupled to the sampling outlet of the filtration module. A method of sampling during a bioprocess including providing such a filtration module, urging a process medium through the process flow path, filtering the process medium by using the filter membrane, extracting a sample from the process medium by using the sampling membrane, and guiding the extracted sample to a sampling outlet.

A filtration module for filtering a process medium in a bioprocess including a process flow path for a process medium, a filter membrane coupled to the process flow path, and a sampling membrane coupled both to the process flow path and to a sampling flow path for extracting a sample from the process medium. The sampling flow path guides the extracted sample to a sampling outlet of the filtration module or to an analyzer integrated into the filtration module. A filtration assembly including the filtration module and an analyzer coupled to the sampling outlet of the filtration module. A method of sampling during a bioprocess including providing such a filtration module, urging a process medium through the process flow path, filtering the process medium by using the filter membrane, extracting a sample from the process medium by using the sampling membrane, and guiding the extracted sample to a sampling outlet.

The present disclosure provides systems and methods that can treat feeds with elevated organic levels, e.g., feeds with ≥300 Pascals (Pa) organic osmotic pressure, with one or more enhanced filter membrane modules, which may be referred to herein as membrane modules or simply modules. Preferably, a filter membrane module consistent with the present disclosure include one or more plate and frame modules, one or more spiral format modules, or a combination of plate a frame and spiral format modules. The systems and methods provided herein can provide reliable performance when used to treat feeds with elevated organic levels.

A flow plate for a humidifier, having flow fields on both mutually opposite flat sides of the flow plate is described. The flow plate proposed here has a multiplicity of through-openings, wherein the through-openings are designed such that a perpendicular projection of the through openings onto a plane oriented parallel to the plane of the flat surface of the flow plate has a non-vanishing area, so that gas passing through the through-openings effects, at least in part, mixing of a gas guided in the flow fields perpendicular to the plane of the flat surface of the flow plate. The through-openings improve the power of the humidifier, thus permitting a lower number of flow plates and therefore a more lightweight and more compact design.

The invention concerns a filtration assembly (1) for microbiological testing and a method of using the filtration assembly for that purpose. The filtration assembly (1) comprises a ring-like membrane support (10) holding a filtration membrane (11), a cylindrical reservoir (20) of which opposite axial ends have openings and one axial opening is removably and fluid-tightly attachable to the membrane support (10) to define a sample volume adjacent to the filtration membrane (11) on one axial side of the membrane support (10); and a drain member (30) removably and fluid tightly attachable to the membrane support (10) to define a drain channel space adjacent to the filtration membrane (11) on an opposite axial side of the membrane support (10).