A method for filtering a gas includes delivering a gas into a compartment of a gas filter assembly; applying a partial vacuum to the gas filter assembly so that the partial vacuum assists in drawing the gas through a porous filter body of the gas filter assembly that is at least partially disposed within the compartment of the gas filter assembly; and regulating the application of the partial vacuum based on a pressure reading of the gas upstream or downstream of the gas filter assembly.

A liquid mixing system includes a support housing at least partially bounding a compartment. A mount is secured to the support housing. A drive motor assembly is configured to engage a drive shaft for moving the drive shaft within the compartment of the support housing. A four bar linkage system extends between the mount and the drive motor assembly, the four bar linkage system being movable between a first position wherein the drive motor assembly is disposed at a first elevation and a second position wherein the drive motor assembly is disposed at a second elevation that is different from the first elevation.

System and method for exercising cells and/or tissue in a sealed bioreactor. System includes a cartridge having a stretching means and a means to retain cells on a scaffold mounted within the cartridge during seeding. System includes a bioreactor including a sealed enclosure, the sealed enclosure housing the scaffold and the cartridge, the bioreactor enabling uniform seeding of the scaffold with the cells, the seeding occurring within the sealed enclosure to protect from environmental contamination. The bioreactor system provides a means to supply fresh media to the cells and/or tissue, and a means to remove waste products.

An in vitro microfluidic intestine on-chip is described herein that mimics the structure and at least one function of specific areas of the gastrointestinal system in vivo. In particular, a multicellular, layered, microfluidic intestinal cell culture, which is some embodiments is derived from patient's enteroids-derived cells, is described comprising L cells, allowing for interactions between L cells and gastrointestinal epithelial cells, endothelial cells and immune cells. This in vitro microfluidic system can be used for modeling inflammatory gastrointestinal autoimmune tissue, e.g., diabetes, obesity, intestinal insufficiency and other inflammatory gastrointestinal disorders. These multicellular-layered microfluidic intestine on-chips further allow for comparisons between types of gastrointestinal tissues, e.g., small intestinal duodenum, small intestinal jejunum, small intestinal ileum, large intestinal colon, etc., and between disease states of gastrointestinal tissue, i.e. healthy, pre-disease and diseased areas. Additionally, these microfluidic gut-on-chips allow identification of cells and cellular derived factors driving disease states and drug testing for reducing inflammation.

The present disclosure provides a delivery consumable for delivering a fluid to a bioreactor. The delivery consumable comprises a container including a collapsible portion comprising a collapsible wall, and an intermediate portion connected to the collapsible portion and being adapted to hold a fluid. The deliver consumable also comprises a connector adapted to connect the intermediate portion to the bioreactor. The collapsible portion is adapted to collapse and urge the fluid through the connector and into the bioreactor.

An assembly for handling biological material, including a planar interface having at least one port, and a component retaining element, spaced apart from the planar interface, configured to retain a component for handling biological material, in which at least one component chosen from the planar interface and the component retaining element is moveable to bring the port and the component retaining element into registration with one another. The registration between the at least one port and the component retaining element adapted to form a fluid communication pathway may be provided between a component retained by the component retaining element and a container associated with the planar interface through the port.

Disclosed herein are platforms, systems, and methods including a cell culture system that includes a cell culture container comprising a cell culture, the cell culture receiving input cells, a cell imaging subsystem configured to acquire images of the cell culture, a computing subsystem configured to perform a cell culture process on the cell culture according to the images acquired by the cell imaging subsystem, and a cell editing subsystem configured to edit the cell culture to produce output cell products according to the cell culture process.

A liquid mixing system includes a support housing at least partially bounding a compartment. A mount is secured to the support housing. A drive motor assembly is configured to engage a drive shaft for moving the drive shaft within the compartment of the support housing. A four bar linkage system extends between the mount and the drive motor assembly, the four bar linkage system being movable between a first position wherein the drive motor assembly is disposed at a first elevation and a second position wherein the drive motor assembly is disposed at a second elevation that is different from the first elevation.

A filtration assembly is provided, comprising a reservoir for holding a sample to be filtered, the reservoir having open top and bottom ends, and inwardly facing arms arranged at the bottom end, the reservoir having an elastic side wall; a fluid port in fluid communication with the reservoir; a porous microorganism-capturing filter element disposed across a flow path between the reservoir and the port, the filter element being releasably retained by the inwardly facing arms; an absorbent pad arranged below the filtration element and the inwardly facing arms, disposed across the flow path between the reservoir and the port; a base detachably mounted to the reservoir, the base including the port, and a support surface for supporting the pad; wherein compressing the elastic side wall releases the filter element from the inwardly facing arms after the base is detached from the reservoir.

Described herein are apparatuses and methods for culturing and monitoring cells in dynamic physiological conditions with combinatorial and biomechanical stimulation. In some embodiments, the apparatuses and methods may comprise one or more cell culture chambers, flexible membranes, pneumatic actuators, microfluidic layers, or hydrogels. In some embodiments, various mechanical stimuli including bending stress, shear stress, or a combination thereof may be applied to one or more cell types. Also described herein are high-throughput and dynamic cell culture array systems comprising the described apparatuses and methods.