A method for removing exhaust gas from a bioreactor (3) and a bioreactor system. The method comprises the steps of: —providing at least one exhaust filter (15; 115a, 115b) connected to an outlet (7) of the bioreactor (3) for transferring exhaust gas out from the bioreactor; —increasing a pressure at an inlet side (25) of the at least one exhaust filter (15; 115a, 115b) in a connection (16) between the bioreactor (3) and the at least one exhaust filter (15; 115a, 115b) or decreasing a pressure at an outlet side (23) of the at least one exhaust filter (15; 115a, 115b).

There is provided an accommodation case (1) having a first wall part (33) in which a power supply unit (40) that transmits electric power to a power supply destination in a noncontact state is provided, a second wall part (34) in which a power reception unit (50) that receives electric power that is supplied from a power supply source in a noncontact state is provided, where the second wall part (34) faces the first wall part (33), and an accommodation space (35) that is surrounded by a plurality of wall parts including the first wall part (33) and the second wall part (34).

A cellbag bioreactor includes a stacked filter providing multiple porous membranes to define a filter cavity. Additionally, a filter within the cellbag bioreactor may be tethered so as to help maintain each membrane of a filter wetted during bioreactor operations.

A tool for fixating and handling membrane-shaped tissue for research or clinical use includes a platform having a base plate with at least one positioning element for positioning a spanning element on the platform, at least one round shaped spanning element adapted for being positioned on the platform using the positioning element, at least one flexible element for positioning over the round shaped spanning element for spanning the membrane shaped tissue, and at least one handling means for handling the flexible element during positioning of the flexible element over the round shaped spanning element, and for handling the combination of the round shaped spanning element and the flexible element, when the membrane is spanned over the round shaped spanning element.

In the production of a culture vessel in which a low cell-adhesive polymer as a coating agent is applied to a culture surface having a plurality of concave parts formed thereon, a use amount of the coating agent can be reduced. The low cell-adhesive polymer as the coating agent is applied to a surface of a culture base material in advance, and subsequently the culture base material is subjected to processing to form the culture vessel having the surface of the culture base material coated with the coating agent as the culture surface.

The present invention relates to collapsible and/or foldable fermentation and/or culture vessels fabricated of an adjustable frame including sections of gas permeable material or in the alternative a non-rigid gas permeable polymeric container or bag fabricated of either a gas permeable or non-gas permeable material with the further benefit of more efficient inventory space and disposal space, wherein the gas permeable material or non-gas permeable material comprises an analyte or pH sensing material integrated or impregnated into at least one section of the material.

A cell culture apparatus includes an introduction-side flow path arranged to allow a culture solution introduced to flow therethrough and be introduced therethrough into each of a plurality of concave wells of a flexible strip circumferentially wound, and a first introduction-side seal provided on an outer circumferential side of the introduction-side flow path, the first introduction-side seal being configured to block flow of the culture solution from the introduction-side flow path to an outer circumferential side of the flexible strip.

Systems and methods for containing and manipulating liquids, including vessels and unit operations or components of cell culture, cell containment, bioreactor, and/or pharmaceutical manufacturing systems, are provided. In certain embodiments, such vessels and unit operations are directed to continuous perfusion reactor or bioreactor systems and may include one or more disposable components. For instance, in one aspect, a system includes an apparatus in the form of a bioreactor for harvesting cells which produce one or more products. The apparatus may include a disposable, collapsible bag adapted for containing a liquid, the collapsible bag in fluid communication with a liquid-solids (e.g., cell) separation device. For example, an outlet of the collapsible bag may be connected to an inlet of the separation device, and an outlet of the separation device may be connected to an inlet of the collapsible bag for recycle. Accordingly, after separating the cells from the liquid in the separation device, the cells can be flowed back into the collapsible bag where they can be re-harvested. Meanwhile, product contained in the liquid can be collected in a separate container. The efficiency of product formation in such a system may be enhanced by using mixing systems described herein.

In one aspect, provided is a composition (biomimetic composition) that includes a biomimetic in vitro model of an arteriolar vessel comprising: at least one of 1) human smooth muscle cells and 2) human pulmonary endothelial cells; wherein the vessel recapitulates one or more of the overall tubular geometry, morphometrics, extracellular matrix constituents, cellular morphology, cellular alignment, and functional heterotypic connections between the human smooth muscle cells and/or the human endothelial cells as compared to an in vivo arteriolar vessel. A microfluidics-based model platform of the pulmonary circulation is provided. Methods of use include measuring flow in biomimetic vessels, and to determine the resistance of these biomimetic vessels in the setting of a variety of experimental conditions that recapitulate the pathobiology of pulmonary hypertension.

A biological component treatment system includes a biological component kit having tubes that allow a liquid to flow therethrough and a biological component cassette, and a biological component treatment device. The biological component cassette includes flow paths in the interior thereof through which the liquid is allowed to flow, and is equipped with a cassette main body formed in a sheet shape that possesses flexibility. The cassette main body includes a liquid level target detection unit that causes a liquid level of the liquid to be detected. A cross-sectional area of a storage space of the liquid level target detection unit is greater than a cross-sectional area of the flow paths.