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.

Proposed are a three-dimensional structuring method of cells and a three-dimensional structuring system of cells capable of efficiently bonding multiple cell clusters in a three-dimensional direction, pursuant to their growth, while ensuring safety. A plurality of fibers, in which one end of each of the fibers is held by a flat plate, are inserted together with the flat plate into a flow path through which a culture solution is supplied, a plurality of cell clusters are placed in the flow path upon causing the cell clusters to run with a liquid flow of the culture solution, and each of the cell clusters is cultured by being stacked on an outer surface of each of the fibers with the flat plate as a growth origin.

A culture device includes a culture vessel that contains a culture solution for culturing cells, a gas supply device that supplies a gas to the culture vessel, and a humidification device that humidifies the gas flowing from the gas supply device to the culture vessel. The humidification device includes a hollow fiber membrane filter that includes a hollow fiber membrane through which the gas from the gas supply device passes and a casing that accommodates the hollow fiber membrane, a water supply device that fills the casing of the hollow fiber membrane filter with water, and a first heater that heats the hollow fiber membrane filter.

The present invention relates to a device (100) for monitoring the development of a biological material, said device in the orientation intended for use comprising: a housing (2) having an extension in a longitudinal direction (X) and an extension in a transversal direction (Y), said housing comprises: two or more culture dish compartments (4), each adapted to accommodate a culture dish (6) comprising a biological material (8) to be monitored, each said compartment being separated from each of said other compartments, said two or more compartments being arranged along the longitudinal direction; each said culture dish compartment (4) comprising a lid (10) adapted to be able to be shifted between an open configuration in which access to the interior (12) of said culture dish compartment is provided, and a closed configuration sealing off the interior of said culture dish compartment from its surroundings; wherein each said culture dish compartment comprises an inlet (14) for supplying gas to and an outlet (16) for removing gas from said culture dish compartment; wherein each said culture dish compartment comprising heating means (18) for heating the interior of said culture dish compartment; wherein said housing comprises one or more cameras (20) for capturing images of a biological material in a culture dish.

Methods, systems, and devices for non-invasive measurement of cell cultures are described that provide for remote monitoring of cell status. The system includes a cell culture vessel, at least one monitoring layer, at least one measurement device, and a communication component. The cell culture vessel may include at least one cell culture chamber configured for cell growth and for closed-system operation. The monitoring layer is external to the at least one cell culture chamber. In some cases, the communication component is configured to transmit data from the monitoring layer to a remote location.

Cell culture systems and methods provide improved immunotherapeutic product manufacturing with greater scalability, flexibility, and automation. Cell culture systems are configured with interchangeable cartridges, allowing versatility and scalability. Systems are configured to have multiple connected cell culture chambers, which allows parallel processing of different types of cells. Gas-impermeable cell culture chambers and methods for generating cells in closed systems prevent contamination and user error. Methods for recycling cell culture medium provide additional efficiencies.

The present invention involves a fill needle system for aseptically dispensing a pharmaceutical fluid in an aseptic chamber comprises a fill needle tubing in fluid communication with a pharmaceutical fluid source via flexible tubing and extending through a fill needle hub; a fill needle dispensing tip disposed at a dispensing end of the fill needle tubing; a fill needle sheath shaped and arranged to removably mate with and seal aseptically to the fill needle hub to form an aseptically sealed volume enclosing the dispensing tip; and a fluid pressure pulse induction system disposed and configured to compress the flexible tubing in order to dislodge droplets of pharmaceutical fluid retained on the dispensing tip after halting dispensing of the pharmaceutical fluid. An associated method of dispensing pharmaceutical fluid comprises operating the fluid pressure pulse induction system to dislodge the droplets. The system may comprise a controller for automatically controlling the dispensing and droplet dislodging.

Embodiments of a method of modulating a potency level phenotype of a source population of cells include culturing the source cell population in a liquid medium within a cell culture incubator, the incubator is configured to independently regulate one or more variable parameters of gaseous conditions within the incubator, the more than one variable atmospheric parameters within the incubator being regulated independently of each other and independently of ambient external gaseous conditions. The method further includes regulating the one or more variable parameters of the gaseous condition within the incubator such that at least one of the one or more variable parameter differs from an ambient level of the respective variable parameter, and as a consequence of such difference from ambient conditions, the subset population is driven from a first potency level phenotype to a second potency level phenotype. In these method embodiments, the first phenotype of the subset cell population is expressed under a gaseous condition absent the regulation of the one or more variable parameters of the gaseous condition, and the second phenotype of the subset cell population is expressed as a consequence of exposure to the gaseous condition as determined by the regulation of the two or more parameters of the gaseous conditions within the incubator.

A system for controlling the development of a culture in solid medium in a robotised incubator (100), having an imaging system (1) configured to take images without moving a Petri dish (5) from the location in which the culture is carried out, and a system for analysing the images obtained by the imaging system, wherein, on the basis of the information provided by the system for analysing the images from the imaging system, which analyses the images provided by the imaging system by a growth detection algorithm, the development of the culture in an incubator (100) is determined, without moving the Petri dish (5) from the location in which the culture is carried out.

A cell deposition and imaging apparatus comprises: a printing mechanism comprising at least one channel, the at least one channel of the printing mechanism arranged to: receive a sample of a cell-carrying fluid comprising at least one cell-type; and deposit the sample of the cell-carrying fluid onto a target area of a substrate, an imaging system arranged to image the target area; and a transportation system arranged to move the target area between a printing position, in which the target area is located substantially adjacent to the printing mechanism, and an imaging position, in which the target area is located substantially adjacent to the imaging system; wherein the imaging system comprises an imager capable of imaging a region of the substrate wherein the region is smaller than the target area and the imaging system is arranged to image all of the target area by moving the target area relative to the imager.