In accordance with an embodiment, a microfluidic chip including a first cells enrichment system and a second cells enrichment system is provided. Channel layouts of the first and the second cells enrichment systems are symmetric with respect to a reflection plane vertical to the microfluidic chip. Each of the first the second cells enrichment systems includes a first fluid channel, a second fluid channel, a sample channel, an inlet channel, and a filtration chamber. The sample channel of the first cells enrichment system has a first inner wall and a first outer wall. The sample channel of the second cells enrichment system has a second inner wall and a second outer wall. The first outer wall and the second outer wall are both far from the reflection plane. A distance between the first outer wall and the second outer wall is in the range from about 10 m to about 1 cm.

A micro-fluidic system for a perfusion cell culture is disclosed. The system includes: a substrate; a micro-fluid injection channel defined in the substrate to guide fluid in a plane direction of the substrate; at least two micro-fluid branch channels defined in the substrate, wherein the branch channels are branched from the micro-fluid injection channel; micro-fluid outlet channels defined in the substrate, wherein each of the outlet channels extends from a distal end of each branch channel to a top face of the substrate, wherein each outlet channel has each through-hole defined in the top face portion of the substrate; and well plates disposed on the top face of the substrate, wherein each of the well plates fluid-communicates with each outlet channel. The micro-fluidic system refers to a technique that adjusts a flow of liquid or gas of a very small amount (nanoliter or picoliter) in an extremely miniaturized device.

A method of mixing fluid flowing in a raceway channel is provided which includes directing the fluid to flow over a ramp which extends across the raceway channel. The ramp has a leading surface which is inclined at between about 5 and 45 upwardly to a top edge, and a trailing surface which extends vertically downwardly from the top edge. The height of the ramp is selected so that the top edge is lower than the level of the fluid in the raceway channel.

A tank receives, mixes, and dispenses input materials including algae feed stock, a micro-nutrients, cleaning solution, a sterile gas, a heating/cooling fluid, carbon dioxide, and raw water with a water treatment system. A plurality of output stations include a vent to atmosphere, a heating/cooling media return, a cleaning disposal, and an algae concentrate/product. The vent to atmosphere is coupled to the tank. The heating/cooling media return is coupled to the heating/cooling media supply through the tank. The cleaning solution disposal station is coupled to the tank with a pump followed by a nano bubbler and an algae growing system. An algae concentrate/product station is coupled to the tank. An algae dewatering system is intermediate the tank and the algae concentrate/product. A water return line couples the algae dewatering system and the water treatment system.

A system for performing a gas-liquid mass transfer includes a container bounding a compartment and having a top wall, a bottom wall, and an encircling sidewall extending therebetween. A tube has a first end and an opposing second end, the first end of the tube being disposed within the compartment of the container. A nozzle is disposed within the compartment of the container and has at least one outlet, the nozzle being coupled with the tube so that a gas can be passed through the tube and out the at least one outlet of the nozzle. The nozzle is sufficiently buoyant so that when a fluid is disposed within the compartment of the container, the nozzle floats on the fluid.

Methods and compositions for long term continuous flow fermentation using a two vessel continuous culture fermentation apparatus are described.

A cell culture device includes a culture unit, a gas supply unit, a first pressure unit, at least one inspecting unit and a control unit. The culture unit contains a cell culture liquid. The gas supply unit, connected with the culture unit, is used for transmitting a culture gas into the culture unit. The first pressure unit, connected with the culture unit, is used for applying a pressure to the cell culture liquid in the culture unit. The at least one inspecting unit, connected with the culture unit, is used for receiving the cell culture liquid for inspection. The control unit, electrically coupled with the culture unit, the first pressure unit, the gas supply unit and the at least one inspecting unit, is used for monitoring corresponding condition parameters to determine respective operations. In addition, a cell culture method for the cell culture device is also provided.

A method is provided for monitoring a flow behavior of mixed components without requiring additional instrumentation or sampling. The method is carried out by determining ratios of the power required to rotate a mixing impeller at different rotational speeds and then comparing the ratios. Characteristics about the mixed components are determined based on differences between the ratios.

Disclosed is an ultrahigh-pressure homogenizing integrated device and a cell disruptor. The ultrahigh-pressure homogenizing integrated device includes a long oil cylinder, a main connecting sleeve, a high-pressure cylinder homogenizing main body, an auxiliary connecting sleeve and a short oil cylinder, which are sequentially and coaxially arranged. An upper part of the high-pressure cylinder homogenizing main body is provided with a feeding hole communicated with a high-pressure cavity; and the feeding hole is connected with an integrated feeding device. A pressurizing plunger rod in the high-pressure cavity of the high-pressure cylinder homogenizing main body is connected with a piston rod of the long oil cylinder; and a homogenizing valve arranged in the inner cavity, which is communicated with the high-pressure cavity, of the high-pressure cylinder homogenizing main body, is connected with an ejector rod of the short oil cylinder.

A culture medium preparator includes a cylindrical vessel that terminates at the low part in a substantially hemispherical cap, a lid and a stirrer placed in the vessel. The stirrer includes a vertical tube placed in the center of the vessel, a plurality of blades put into rotation about the tube and magnetic masses at the periphery so that they are placed in proximity to the internal wall of the vessel. The preparator furthermore includes a magnetic ring in rotation about the internal wall at the same height as the magnetic masses. The magnets attract the magnetic masses, the magnetic ring being moved in rotation by a motor. In this way, the stirrer is driven in rotation without requiring mechanical elements placed inside the vessel, the absence of such elements facilitating the cleaning.