Sensors are configured to capture measurement data representing dissolved oxygen (DO) measurements of an environment and capacitance measurements of a medium of the environment. A memory includes computer-executable instructions. One or more processors are communicatively coupled to the one or more sensors and configured to execute the computer-executable instructions to carry out operations comprising: generating, using first measurement data captured by the one or more sensors, a model based on a relationship between the first set of DO measurements and the first set of capacitance measurements; receiving, from the one or more sensors, second measurement data; predicting, using the model and based on the new capacitance measurement, an expected DO measurement; determining whether to use the expected DO measurement or the new DO measurement; and controlling, a valve to cause the determined oxygen input amount to flow into the environment based on the expected DO measurement.

An electrochemical measurement device for measuring a chemical substance generated or consumed in a biological sample in a solution includes electrode surfaces, a spacer, and at least one wall plate. The electrode surfaces, the spacer, and the wall plate are arranged on the same flat surface. Each of the electrode surfaces has a diameter d.sub.el not more than 80 μm. A height of the spacer has a predetermined value within a range given by h=21.8(d.sub.el+0.8)/(d.sub.el+9.7)±5 [μm]. The spacer has a structure in which an enclosed three-dimensional region is not formed by the biological sample, the flat surface, and the spacer while the biological sample is in contact with the spacer. The wall plate has a property of being impervious to a dissolved substance in the solution and has a height not less than the height of the spacer. Two of the electrode surfaces are separated by the wall plate.

Aspect of the disclosure relate to methods of assessing a bioreactor culture that involve determining a culture parameter of the manufacturing-scale bioreactor culture using a model that relates a Raman spectrum to the culture parameter. Related bioreactor system are also provided.

According to the invention, there is provided a parallel bioreactor system, comprising: an oscillator for generating oscillating motion; a plurality of culture vessels mounted on the oscillator, wherein each culture vessel is provided with an inner cavity, the inner cavity comprises a cylindrical portion at the upper part and an inverted truncated conical bottom at the lower part, a cross section of the cylindrical portion is consistent with the cross section of the top of the inverted truncated conical bottom, and the bottom of the cylindrical portion is joined with the top of the inverted truncated conical bottom; disposable culture bags arranged in the inner cavities of the culture vessels and used for accommodating culture solution, wherein each disposable culture bag is provided with a multifunctional cover plate, and the multifunctional cover plate is connected to the top of the culture bag to seal the culture bag, and is provided with a plurality of connection holes leading to interior of the disposable culture bag; and a control system, wherein the control system controls the oscillating motion of the oscillator and parameters of the culture solution in the disposable culture bags.

The invention is comprised among control devices for controlling and monitoring fluids and for the handling thereof. The invention relates to the integration of these control devices in a disposable cartridge cooperating with a platform for a system for monitoring and controlling a fluid. Specifically, the invention relates to a disposable cartridge and a platform, cooperating with one another, for a system for monitoring and controlling the state of a fluid, wherein the cartridge comprises at least two sensors. The invention also relates to a system and installation for monitoring and controlling the state of a fluid. More particularly, the present invention is intended for monitoring and controlling the state of a cell culture.

A microbial sensor, system and method that can be used to determine the chemical environment and/or substrate concentrations in saturated and unsaturated natural and environments, such as soils, aquifers and sediments are disclosed. The system may be used for monitoring municipal and industrial treatment facilities and sites where chemicals or contaminants were released to natural environments. The electrochemical microbial sensor system can be referenced using either a cathode exposed to oxygen or a reference cell (silver/silver chloride or calomel) for monitoring natural or man-made environments.

A device for storing live algae is disclosed. The device may include: a closed container, at least partially transparent to light, the container is configured to hold live algae aquaculture at a predetermined temperature; at least one light source for providing light to the closed container; a CO.sub.2 source for providing CO.sub.2 to the closed container; an air circulation system for circulating air inside the closed container; and a controller for controlling the at least one light source to illuminate an internal space of the closed container in an amount sufficient to keep the algae aquaculture alive but inhibits reproduction of the algae for at least 4 weeks.

Systems and methods for automated cell culturing are disclosed. In some embodiments, one or more cell culture vessels are fluidly connected with one or more multiport valves and one or more fluid pumps. The fluid pumps may pump various fluids into and out of the cell culture vessels as necessary to support cell growth, routed by the one or more multiport valves. In some embodiments, one or more components may be removable from other components so that some components may be prepared and sterilized independently prior to usage.

In a culture container including a plurality of recesses for culturing a culture target, such as spheres, a liquid substance can flow between the recesses and the movement of the culture target between the recesses can be prevented. A culture container includes a plurality of recesses for accommodating a culture target, the culture container including a container body having a first surface in which the recesses are formed, and a top plate having a second surface facing the first surface, protrusion portions and/or channel portions being provided on a side of the first surface and/or a side of the second surface, the container body being in contact with a part of the top plate to form a channel between the container body and the top plate, and a width of the channel being smaller than a minimum diameter of the culture target.

To estimate concentration of a cellular metabolite contained in a culture medium where certain cells are cultured, using a simple method, etc., spectroscopy. The number of the certain cells is estimatable by applying previously obtained information regarding relationship between a cellular metabolite concentration and the number of the certain cells.

In spectroscopy, the higher the cellular metabolite concentration, the more accurately the actual concentration of the cell consumed-substance can be estimated. Accordingly, the concentration of a cell-consumed substance, decreasing as cells are cultured, are estimated in the early to middle stages of culture, and the concentrations of a cell-produced substance, increasing as cells are cultured, are estimated in the middle to late stage of the culture. This enables estimation of the number of cells in the entire range from beginning to end of cell culture.